In order to increase the knowledge of veterinary drug rights protection and protect the interests of farmers, several methods for the identification of counterfeit veterinary drugs are introduced below and are for reference only. 1. Check whether veterinary drug manufacturers have been approved. The label specification of a legal veterinary drug manufacturer should mark the production license number. Veterinary drugs produced by any unnamed or unapproved unit must be fake veterinary drugs. You can check the Chinese Veterinary Drug Information Network (http://). 2, check the product approval number. (1) Look first for the approval number of the product, and then see if the format of the approval number is correct. (2) Look at whether the approval number is within the validity period (valid for 5 years). If it is not within the validity period, it will be fake veterinary medicine. The four Arabic numerals in brackets in the approval number are the years when the approval number was approved, and the years marked with the production lot number (ie the date of production) should not exceed the approval year of the approval number plus five years. 13, please check the competent authorities. The veterinary administrative department at or above the county level or a veterinary drug inspection agency at or above the provincial level may be required to perform identification or inspection to distinguish between genuine and fake veterinary drugs, and may also report production, operation, and use of counterfeit veterinary drugs to them (Guangdong Provincial Department of Agriculture -37288285) so that the administrative authorities can punish illegal activities to protect the legitimate interests of consumers.
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3, check the product specifications. To see if the specifications marked on the label are in line with the actual situation of the drug, it depends mainly on whether the labeling volume matches the actual volume.
4, check the name of veterinary drugs. Including the legal name (also known as: common name) such as national standards, provincial local standards (Note: Before the Ministry of Agriculture officially announced the abolition of provincial local standards, the provincial local standards are still valid. The same below) The name of the veterinary drugs contained in the Trade names, legal titles may not be marked as trademarks. Labels, instructions, and packaging must be printed with the legal name of the veterinary drug product, and the existing product name should be printed at the same time.
5, check the implementation of standards for veterinary drug products. Veterinary drug standards should implement national standards (Chinese Veterinary Pharmacopoeia, Ministry of Agriculture standards) or provincial-level local standards. If veterinary drug ingredients do not comply with national standards or provincial-level local standards, they are counterfeit drugs.
6, check the validity of veterinary drug products. Whether the veterinary drug product indicated in the label's specification exceeds the validity period or exceeds the valid period can be judged as inferior medicine.
7. Check if it belongs to veterinary drugs that are prohibited or eliminated by the state. Isoprenaline drugs are veterinary drugs that are banned by the state; hydrochloric acid hydrochloride injection, 2% or 4% aminopyrine injections are all culls of veterinary drugs.
8, check veterinary drug labels, instructions. The veterinary drug packaging must be labelled with the words "veterinary use" and instructions. Labels or instructions must be marked with registered trademarks, veterinary drug names, specifications, company names, product lot numbers and approval numbers, main components, contents, roles, uses, usages, amounts, expiry date, and precautions. If the withdrawal period is specified, it should be stated on the label or the instruction manual.
9, check the veterinary drug product quality inspection certificate. A veterinary drug package should be accompanied by a product quality inspection certificate. No certificate may not be delivered, and a veterinary drug business unit may not sell.
10, check the appearance of the tablet to be clean, uniform color, and have the appropriate hardness. Ordinary white tablets that appear discolored, moldy, loose, damp, sticky, rough surface, or crystallized, indicating that the tablets have deteriorated and must not be used.
11. The dispersant should be dry, loose, mixed, and uniform in color. If the agglomerate is severe, deliquescence or liquefaction and discoloration, the drug has deteriorated.
12. Check veterinary injections for multiple injections and injections. Injections are mainly identified from the clarity and color checks. Clarity check: In addition to special varieties, water injections should be uniform and clear. If any turbidity, sedimentation, floc, or Other foreign materials appear, it indicates that the drug has deteriorated. Color inspection: The color of the injection changes, indicating that the drug has undergone chemical changes; when the color changes significantly beyond the specified limit, can not be used. Powder injections are mainly antibiotics such as penicillin and streptomycin. Normal powder injections should be allowed to freely turn in the bottle, colorless spots, and foreign matter. If there is discoloration or shaking of the color point, the powder will stick to the bottle and even cause deliquescence and agglomeration. , should be regarded as product deterioration, can not be used.