1. What is medicine? -
medicine is used for prevention. treat. diagnosis of human diseases. purposeful regulation of human physiological function, and provides for indications or functions. usage and consumption of substances. -
2. medicines include? -
include Chinese herbal medicine. Chinese Herbal Medicine. medicine. chemicals and their formulations of antibiotics. biochemical drugs. radioactive pharmaceuticals, serum of the vaccine. blood products and diagnostic medicine. -
3. four of the drugs? -
a. Specificity; b. duality; c. the importance of quality; d. limit of drugs. -
4. national drug standards include? -
a. -
5. Chinese medicine: Chinese herbal medicine and Chinese medicine in general and Pieces. -
6. medicine: mainly refers to the method of chemical synthesis, or extracted from natural products made of the active ingredients of the drug. -
7. medicine: the one or more drugs as raw material made of a certain dosage forms, and the other from the popular proper names, may, without directly for prescription drugs used in patients. -
8. Health and Medicine: All plants and animals. parts or secretions formed by simple processing of drugs, such as rhubarb. musk. -
9. bio-chemical: means from animals plants and microorganisms in the extraction and separation of natural substances, including the use of biosynthesis and chemical synthesis prepared by the above-mentioned substances. -
10. Biological Products: refers to microbiology. immunology and biochemistry of the theory and method for producing the vaccine of the vaccine. toxoid. antitoxin and blood products. -
11. drug: refers to the chemical structure or composition of the role and some drugs are not known and there are some clinical value or significance of the drug theory. -
special drug: refers to the specific purposes of the drugs, including diagnostic treatment, specific antidote. Ophthalmology, Dermatology. Obstetrics and Gynecology. dental medicine and so on. -
12. common types of dosage forms: injections. tablets. solution agent. syrups. suppositories. ointments. capsules. aerosols. pills. granules. -
13. According to the source of drugs are divided into: natural categories. chemical class of mixed classes. -
14. According to the chemical composition of drugs can be divided into: organic drugs class. inorganic pharmaceutical class. crude drug class of other classes of biological drugs. -
15. the national drug standards, the State designated to ensure the quality of drug quality indicators such as test methods and technical requirements of the production process, including the State Drug Administration promulgated the pharmaceutical standards. -
16. drugs and non-drugs. internal medicine and external medicine should be stored separately; easy to odor of drugs. medicines. Chinese Herbal Medicine and other dangerous goods should be kept separate from other drugs. -
17. State of the drugs for what kind of classification system? -
implementation of prescription and non prescription drugs classification system. -
18. What is a prescription drug? -
is the virtue of practicing doctors and assistant doctors prescription to purchase, deployment and use of drugs. -
19. What non-prescription drugs? -
is the department by the State Drug Administration announced not by virtue of practicing doctors and assistant doctors prescription, consumers can judge for themselves, purchase and use of drugs. -
20. What is fake? -
According to such drugs. -
21. one of the following circumstances drugs, counterfeit punished by: (1) drug regulatory department under the State Council banned the use of; (2) In accordance with this Law must approve the production of import, or in accordance with this Law must be Inspection and testing that is not sold; (3). deterioration; (4). to be contaminated; (5) Use in accordance with this Law must obtain approval of the text without approval number to obtain the raw material drug production; ( 6) indicated the indications or functions beyond the scope of the provisions. -
22. What is inferior? -
According to -
23. one of the following conditions of drugs, punishable by inferior quality: (1) does not indicate the period or change the period of validity; (2) does not specify or change production batches; (3) over period of; (4) Direct contact with drug packaging materials and containers unauthorized; (5). without added colorants. preservative. spices. flavoring agents and excipients; (6) Other provisions do not meet pharmaceutical standards of. -
24. What is the lot of drugs? -
batch is a group of approved drug identification number or letters combined with figures. To trace and examine the history of the batch production of drugs. -
25. What is the drug manufacturers? -
pharmaceutical enterprises is the business franchise pharmaceutical companies or sideline business. -
26. the conditions for the establishment of pharmaceutical enterprises? -
enterprises subject to up pharmaceutical enterprises of the province. autonomous. municipalities and Drug Administration approved the issuance to the -
27.GSP mean? -
GSP is -
28. pharmaceutical wholesale business division of the scale of meaning? -
large enterprises with annual sales of 200 million yuan or more drugs; medium-sized enterprises, the annual pharmaceutical sales 50 million yuan to 20,000 yuan; small businesses with annual sales of 50 million yuan the following drugs. -
29. what is the drug mode of operation? Several pharmaceutical sub-mode of operation? -
drugs mode of operation is the Mode of operation of the wholesale medicines. Retail chain and retail three. -
30. can only be purchased wholesale pharmaceutical business for sale to qualified status of drug production. enterprises and the use of units, shall not sell drugs directly to patients or other consumers. -
40. What is the pharmaceutical business scope? -
pharmaceutical business scope is the -
41. enterprises can range management? -
can not, -
42. Our company's quality policy? -
I always adhere to -
43. the quality of leadership and organization structure members? -
quality leadership and organization members should purchase. sales. storage. operators and other business departments directly under the charge and the responsible persons of quality management agencies. -
44. the quality of institutions should be established under the quality management group. the quality of the inspection team, etc., the quality of pharmaceutical quality management agency has the final adjudication. -
45. Quality Acceptance of job duties? -
(1). adhere to the the quality of batch acceptance; (3) Check the packaging of drugs when the response and acceptance. label. instructions and drug certificate and other relevant documents for each checks; (4) acceptance in accordance with the requirements of sampling, taking samples should be representative; (5). inspection and acceptance shall be true and complete record of good inspection and acceptance; (6) acceptance of the first battalion species, should check whether the same drugs factory inspection report; (7) shall, subject to acceptance of drugs places specified, within the prescribed time limit; (8) for acceptance of drugs, in time with the department in the warehouse storage procedures for the handover. -
46. Drug maintenance duties? -
(1). in accordance with the relevant provisions of the enterprise, and storage for storing drugs effective conservation and management of the environment, to ensure the quality of drug storage; (2) the custody officer to guide the rational storage of drugs; (3) Check in the library drug storage conditions, with the custody staff positions such as temperature and humidity between the management of storage conditions; (4) pharmaceuticals inventory regular quality checks and carry out inspection records; (5) according to the characteristics of traditional Chinese medicine and Chinese Herbal Medicine take dry oxygen-. fumigation methods such as conservation; (6) For reasons that may arise due to abnormal quality of medicines and drugs stocks a long time, report to the agency review process of quality management; (7) found in the inspection quality management issues promptly notify the agency review process; (8). periodic summary Analysis and reporting the quality of medicines information maintenance checks; (9). quality management agencies to report regularly to the validity and long-stored drugs in recent reports; (10) responsible for acceptance of maintenance with the equipment. storage facilities management; (11) the establishment of drug maintenance file. -
47. engaged in quality management and acceptance. conservation and measurement of the number of full-time staff working less than 4 staffs of the enterprises, the sum of several types of full-time staff should be not less than three, and remained relatively stable. -
48. What is the pharmacist? -
pharmacist is qualified by the National Examination to obtain -
49. pharmacist is the establishment of pharmaceutical production. operate using one of the prerequisites of the unit. -
50.GSP provides pharmaceutical wholesale business as a responsible person in charge of drug quality and quality management agencies should have the licensed pharmacist or pharmacy professional title corresponding qualifications. -
51. pharmaceutical wholesale enterprises annually organization's quality management. Drug acceptance. conservation. keep direct contact with drugs and other staff positions to conduct health checks, health checks and the establishment of the file. Quality inspection. Maintenance personnel should be increased vision. Achromatopsia inspection items -
52.GSP the requirements of the storage area? -
large enterprise storage area of not less than 1500; medium-sized enterprises not less than 1000; small business not less than 500. -
53. room for inspection maintenance requirements of large enterprises is not an area of less than 50; medium-sized enterprises not less than 40; small business not less than 20 .-
54. places where Chinese Herbal Medicine-packing-packing business, should be fixed packing room, area and equipment should be compatible with the packing requirements; -
55. shipping and receiving areas should be suitable for the demolition of zero and LCL shipments; loading and unloading spaces should ceiling. -
56.GSP environmental requirements for the reservoir? -
(1). reservoir internal environment should be ground flat. easy to repair. no exposed land surface; (2) library district should be fully hardened or green, should not be planted prone to insects. Piaoxu and pollen more easily more flowers and trees to beautify and protect the environment clean; (3) In order to prevent ground water or damp, library area on the ground floor should generally be higher than outside the reservoir area, reservoir area and provision of drainage systems, and to keep them open, the ground should be no water; (4). library district should be clean and tidy environment, no accumulation of garbage waste. -
57. the quality of medicines management in accordance with state requirements, the warehouse should be classified as: library to be tested. Qualified library. consignor library substandard products database. Pieces of Chinese medicine database and returns the zero cargo weighed library. -
58. dangerous goods special management drugs. easy to odor drugs. Pieces of Chinese medicine and Chinese medicine should be set a separate warehouse. -
59. Drug classification according to temperature and humidity conditions of storage and storage requirements, the Treasury is divided into: cold storage (2-10 ℃). cool library (≤ 20 ℃). Library at room temperature (0-30 ℃); relative humidity should be maintained between 45-75. -
60. What is the quality management system documents? Include? -
quality management system documentation is used to ensure the pharmaceutical quality of the document management system;, including enterprise quality management system. the relevant departments and organizations, the quality of job responsibilities. quality management procedures and related records management activities and the original vouchers. -
61. preparation of quality management system documentation should follow the following principles: the principle of legality; practical principles; advanced principles; directive principles; systematic principle; operational principles; to check principle. -
62. the type of quality management system documentation: quality management system; quality management procedures; quality responsibilities; quality records; -
63. What is the first commercial enterprise? -
first commercial enterprise is the first place with the business of supply and demand of drugs or drug pharmaceutical manufacturers enterprises. -
64. What is the first commercial varieties? -
species is the first commercial enterprises to purchase the first time a pharmaceutical drug manufacturers, including drugs, new specifications the new formulations the new packaging. -
65.'s first commercial enterprise the necessary information? -
first commercial enterprise audit requirements must be stamped with the first commercial enterprise to provide a legitimate license a copy of the original seal; drug sales personnel must provide stamped with company original seal and signature of legal representative or power of attorney signed and marked commission mandate and valid; pharmaceutical sales staff ID card; also the first commercial enterprise to provide the relevant proof of quality certification; quality assurance protocol. -
66. The first varieties of essential business information? -
The first camppurchased varieties, the production units of the original should be stamped with the seal to provide a legitimate copy of license; drug quality standards approved pharmaceutical manufacturing documents; first commercial variety of drugs factory inspection report (same batch); drugs packaging label instructions and price approvals and other solid samples. -
67. acceptance of staff should be controlled with the purchase invoices and business quality inspection department issues a notice of storage, inspection procedures in accordance with pharmaceutical medicines for the arrival of batch acceptance. Special management drugs and the implementation of double acceptance of your medicines. -
68. arrival of drugs should be tested area, within the prescribed time limit timely acceptance, general medicine should be two working days after the arrival inspection is completed, the special management of medicines and drugs should be refrigerated after arrival with the that with the experience. -
69. acceptance should be in accordance with the classification of drugs, the drug's packaging. label. manual and related documents required for each certificate or acceptance. -
70. acceptance of the whole package should be the product certification; -
71. acceptance of special management drugs, topical drugs, the packaging label or instructions on the prescribed marking and warning instructions; prescription and non prescription drugs by category management requirements, label instructions are appropriate warnings or advice, etc.; non-prescription drugs packaging is the state's proprietary identification. -
72. acceptance of imported drugs, its internal and external packaging labels should indicate the drug name in Chinese main ingredient, and the registered number, and instructions in Chinese. Direct import of drugs should be on a
73. acceptance of the first camp variety, lot number should be the first arrival of drugs with pharmaceutical factory quality inspection report. -
74. the whole of the acceptance of drugs taken, shall bear clear marks of acceptance sampling, the restoration sealing; -
75. on the acceptance of substandard drugs, medicines should be rejected completing report cards, report review and sign the Quality Management Department of handling, notification service purchase department. -
76. should make drug quality inspection records, the contents of a complete record requirements, no shortage of items, clear writing, a clear conclusion, members of each inspection shall be signed and stamped with acceptance. Inspection records shall be kept valid for one year to more than drugs, but not less than three years. -
acceptance of drugs, acceptance of staff certificates should be signed or sealed storage, and indicate acceptance of conclusions. Storekeeper staff with acceptance certificate signed or sealed storage procedures for storage, the manifest does not match the Quality abnormalities. Loose or damaged packaging. Logo or other problems of fuzzy variety, quality management should be rejected and reported institutions. -
77. in the library drugs for color management? -
Green: qualified pharmaceutical area. go pharmaceutical area; yellow: items to be tested. return drugs area; red: substandard medicines District; -
78. warehouse five anti refers to what? -
dust. moisture. mildew. anti-pollution and anti-pest birds, rodents, etc. -
79. according to the season of climate change, good temperature and humidity control, adhere to a daily on the afternoon of the first to observe and record
80. Inventory lot number and expiration pharmaceutical drugs should be stored in sequence distance burberry uk outlet, different batches of drugs shall not be mixed stack. -
81. position -
the distance between pharmaceutical goods not less than 100 cm; stack and the wall spacing of not less than 30 cm; stack and roof pitch of not less than 30 cm; stack and radiators or heating channel spacing of not less than 30 cm; stack and the ground distance of not less than 10 cm. -
82. drugs produced by the first in first out. recent first-out. batches shipped by the principles of the library. If the first production out of first in first out, and recently there is a conflict, you should follow the recent first-out principle. -
83. drugs for partition, classification management. Specific requirements: (1). Medicines and food of non-pharmaceutical and health category. Internal medicine and external use should be sub-cargo storage; (2) general drug and pesticide rat poison. People medicine and veterinary medicine. Performance affect each other and easy odor of drugs sub-inventory; (3) The special management of medicines to hand care. counter or release of the inventory, management of special accounts; (4) Chinese herbal medicine. Chinese Herbal Medicine should be in accordance with requirements of the different varieties of nature, were set storage Treasury; (5). dangerous drugs should be set release of the inventory, and equipped with suitable security. fire-fighting equipment; (6). Name and confusing variety of packaging stored separately; (7). substandard drugs kept separate and There are obvious signs. -
a library review records should be kept valid for one year to more than drugs, but not less than three years. -
84. out of the library review to find out what the situation should stop shipments, and report quality control department? -
(1). abnormal ring inside pharmaceutical packaging and liquid leakage; (2) the packaging appears damaged. sealing is not strong. liner is not true. serious damage to the seals and other phenomena; (3) packaging does not identify the fuzzy clear or off; (4). medicines has exceeded the expiration date. -
85. What is a library of drugs not allowed? -
(1). expired. rotten bad. infestation. rat-bite and out of drugs; (2) drugs within the packaging is damaged, not finishing the sale; (3) bottles of sign off. pollution ambiguous species; (4). suspect quality changes, without quality control department to clear the status of that species; a return notice or notice to suspend sales of the pharmaceutical sector varieties. -
86. the purchase of notes and bills should be at least ten years of sales. -
special management drugs including toxic drugs for medical use. narcotic drugs. psychotropic substances and radioactive drugs and other four categories. -
87. medicines should be marked valid, or not change the validity period indicated by inferior treatment. -
88. does not indicate the validity of the drugs, storage quality and acceptance shall be deemed to have failed drugs, inspection personnel should reject the goods. -
89. The company provides pharmaceutical nearly valid meaning: from the expiration date deadline less than 12 drugs. -
90. valid for less than six months shall not purchase the drug, not the acceptance of storage. -
91. warehouse is responsible for monthly reporting -
92. Quality Management is the pharmaceutical company responsible for the failure to implement effective control and management of the institution. -
93. shall not purchase substandard quality of drugs. storage and sales. -
94. What does not meet the requirements of the pharmaceutical drugs are substandard? -
(1). quantification (ie determination) results do not meet the statutory requirements of quality standards for drugs: (2) qualitative detection (ie, physical and chemical identification) results do not meet the statutory requirements of quality standards for drugs; (3) Bacterial detection (ie, micro-determination) results do not conform to relevant regulations of the drugs: (4) pharmaceutical packaging. labels and instructions do not conform to relevant regulations of the drugs. -
95. substandard drugs should be required to be scrapped and destroyed. -
96. special management drugs in the loss of nonconforming items in the newspaper should be reported to the local drug regulatory departments. -
97. After the return of all sales of drugs, with sales by the acceptance of staff certificates issued by the return receipt. Drug store and return library in return drugs, hanging yellow logo. -
storage and acceptance in the pharmaceutical discovery process failed drugs, substandard drugs should be stored in the library, hanging red flags reported quality control department. -
98. the quality of their nature and consequences of the accident severity is divided into two major categories of accidents and general accidents. -
99. reflected in consumer complaints of drug quality problems burberry scarves, should be -
100. What is ADR? -
adverse drug reactions is qualified drugs in normal usage. the amount of cases and the drug appears irrelevant to the purpose or unexpected adverse reactions. -
use. toxic reactions and allergic reactions. -
102. the purchase of drugs / selling drugs should be legal bills issued, in accordance with regulations established purchase records, so that ticket. account. things match. Notes and records should be required to keep. -
103. cover the purchase of imported drugs should be obtained with the original supplier and the seal of quality management agency copy, check the legality of imported drugs. -
104. return drugs record keeping for five years. -
105. Acceptance number taken: less than 2 should be piece by piece inspection; 50 the following extract 2; 50 or more, each additional 20, taking an increasing, less than 20 by 20 meter. -
106. taking the smallest packaging: each whole package to extract three samples of the smallest package inspection; that looks abnormal, should be double sampling. -
107. inconsistent with the custodian for the occurrence of a single cargo Quality abnormalities. unsound or damaged packaging. or other suspicious signs fuzzy quality of the drugs, the right to reject, and fill out the -
108. inspection record-keeping to more than one year expiration date, but not less than three years. -
109. acceptance of the package deal drugs. label. manual and related documents required for each inspection, the whole pharmaceutical packaging should be product certification. -
acceptance of Chinese herbal medicine and Chinese Herbal Medicineshould packaging, along with acceptable quality marks. Each package should be marked with the contents of the statutory drug quality. -
110. of narcotic drugs. The first class of psychoactive drugs. toxic drugs for medical use double verification system. -
111. review records should be kept valid for one year to more than drugs, but not less than three years. -
112. shipping drugs should be identified clearly, packaging firm, the number of accurate, stacking neatly packaged medicines must not be inverted. stress, stacking high to moderate. -
113. drug approval number of the format is: Zhunzi letters +8 +1 bit numbers -
114. pharmaceutical drugs purchase records retention period to more than one year but not less than three years, the purchase of recorded drug procurement department fill in and save. -
115. acceptance curing room should be equipped with one-thousandth of the balance. clarity detector. standard colorimetric liquid. Chinese herbal medicine business. Chinese Herbal Medicine moisture analyzer should be configured. Ultraviolet fluorescent microscope or dissection microscope, and shall be equipped with the necessary dust. Moisture equipment. -
116.'s first commercial variety of storage and acceptance should be the first arrival of drugs have the same batch of drugs manufacturers inspection report. -
117. After the return on sales of drugs, regardless of return reason, the procedure should be required batch acceptance. -
118. (1). Pieces of Chinese medicine and Chinese medicine should be packaged, along with acceptable quality marks; (2) each of Chinese herbal medicines should be marked on the package name. origin. date of shipment. supply unit; ( 3) Chinese Herbal Medicine shall be marked on each package name. manufacturer. production date, etc. The label must indicate the name. Specifications. origin. manufacturers. product lot number. production date; (4) implementation of the approval number The Chinese herbal medicine and Chinese Herbal Medicine, shall be marked on the packaging the approval number. -
119. substandard drugs to confirm the report. the reported loss. procedures or destruction of records should be perfect. -
120. quality management agencies responsible for drug quality file creation and management to determine and adjust the quality of medicines variety of file directory, general filing include: first commercial varieties. the main varieties. In addition to the first camp other than the new varieties product variety. varieties of quality problems occurred. Drug Administration monitoring of key species. unstable drug quality varieties of other files necessary to establish quality varieties -
enjoy the near expiration of key drugs conservation, shorter varieties of the statutory limitation period should be established drugs conservation files. -
121. The second category of psychotropic drugs should be stored in a relatively independent of the storage area, and the accounts should be strengthened. cargo management. -
122. the purchase of drugs should be in storage for the first time since three months after the drugs inventory check. -
123. conservation staff on conservation of drugs found during the quality, eye-catching yellow signs to be hung paul smith hats, and suspend delivery, quality of management reporting agency for processing, handling of drug quality problems. -
124. What is the significance for the GSP certification? -
(1). to eliminate quality problems, to ensure safe and effective drugs; (2) improve the overall quality, to ensure that pharmaceutical needs of the community; (3) actively participate in international competition. -
125.GSP the core of what? -
GSP is the core of quality first. -
126. protein assimilation preparations, also known as anabolic hormones, commonly known as anabolic steroids, anabolic drugs, with the promotion of protein synthesis and breakdown of the special permit to reduce the amino acids, can promote muscle proliferation, increase the intensity of the action. -
127. protein assimilation preparations and peptide hormones to keep? -
(1). a dedicated management staff; (2) have special storage warehouse or storage medicine cabinet; (3) have a special inspection, inspection, storage, sale and registration of a storage system; (4) Legal and administrative regulations and other conditions. -
128. protein assimilation preparations. acceptance of peptide hormones. check. custody. sales and registration records should be kept out of storage to more than anabolic agents and peptide hormones valid for 2 years. -
129. how to understand three things off match tickets? -
= the number of drugs purchased inventory has been sold pharmaceutical drugs + number number -
130. Our range of Pharmaceutical Trade License, what? -
Chinese herbal medicine; Chinese Herbal Medicine; medicine; chemical medicine preparation; antibiotics; biochemical drugs; biological products (except vaccines) -
131. put on fine linen and other toxic drugs for any special management inspection system? -
release of the drug hemp and other drugs for double precision inspection system should counter or release of the inventory, double double-lock kept separate accounts records, consistent with the account book. -
132. enterprises sales staff sell drugs, what documents must be issued? -
business license copy, sales staff ID card, the legal representative of the power of attorney, GSP certificate and affix the seal of the company's original sales personnel qualification certificates. -
133. the content of drug labels and instructions What are the requirements? -
labels and instructions must indicate the generic drug name ingredients. Specifications. manufacturer. approval. the product lot number. production date is valid. indications or functions, usage, dosage. contraindication adverse reactions and Note. -
134. warehouse temperature and humidity exceeded how to solve? -
If warehouse temperature and humidity above and below the appropriate standards, should immediately open air cooling or heating, in order to reach the required standards. If the Treasury relative humidity less than 45%, but should be taken to wet mop and other measures, so that the relative humidity higher than 45% or more, if the relative humidity higher than 75% of the Treasury should immediately open exhaust fan dehumidifier. -
135. purchased drugs what should be the first place? -
should be without access to legal qualifications and reputation for quality first. -
136. direct contact with staff must undergo a physical examination every year, and the establishment of health records. -
137.'s internal quality management agencies to the quality of drugs has veto power. -
138. medicines out of the library must be given for quality review procedures. -
139. Drug Name: refers to by the State Food and Drug Administration approval of a specific business use of trade names. -
140. Drug generic name: refers to drugs included in the name of the national drug standards. -
Drug Name Drug Generic Name / Chemical Name -
Ceftriaxone Ceftriaxone -
compound diphenoxylate diphenoxylate tablets -
clomiphene citrate clomiphene citrate capsules -
inflammatory pain meloxicam piroxicam -
brain clear film aminopyrine caffeine tablets -
Ling Tai Bangni nimesulide tablets -
nifedipine nifedipine -
isosorbide dinitrate isosorbide mononitrate tablets -
propranolol propranolol hydrochloride tablets -
mexiletine mexiletine hydrochloride -
spironolactone spironolactone tablets -
amine hydrochloride phenoxybenzamine bamboo pieces -
methimazole Methimazole tablets -
Xishilanxia exposed methenamine solution -
music Halcinonide skin liquid solution -
chlorhexidine acetate, chlorhexidine bolt bolt -
binary out tropicamide eye drops -
enteritis gentamicin bismuth Capsules Capsules -
Venoruton Troxerutin filmXiaozhang film two A silicone sheet -
glibenclamide glyburide tablets -
phenformin phenformin hydrochloride tablets -
amine hydrochloride phenoxybenzamine bamboo pieces -
An asthma compound gallfilm ammonia tablets -
grams of cough sensitivity DIOXOPROMETHAZINE hydrochloride tablets -
tapered needle two hydroxypropyl theophylline injection -
progesterone, medroxyprogesterone acetate tablets -
Women Tablets norethindrone tablets -
one hundred tablets of diphenhydramine ephedrine asthma friends -
sodiumamikacin amikacin sulfate injection -
Glucurolactone glucuronolactone tablets -
love Mauer bromine meter needle that procaine injection -
Pentoxyverine carbetapentane citrate tablets -
security network of blood films adrenal color hydrazone film -
cedilanid deacetylase lanatoside injection -
verapamil verapamil hydrochloride tablets -
vitamin K3 sodium bisulfite menadione tablets -
A acetate, vitamin K4Chennai hydroquinone film -
706 on behalf of the starch-based plasma has 40 hydroxyl sodium chloride -
654-2 film racemic anisodamine hydrochloride tablets -
dipyridamole dipyridamole tablets -
propafenone propafenone hydrochloride tablets -
chondroitin sulfate eye drops corneal Ning -
Xiaoshuan Ling plasminogen injection yzn-
prolactin film compound Vaccaria film -
powerful computer chip Gengnian'an clear Tablets -
periodontal Ning bran sterol tablets -
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