01 2Fujian Fukang Pharmaceutical Co., Ltd. Fuzhou City CN
02 1NORTH CHINA PHARMACEUTICAL GOODSTAR CO., LTD. Chengde CN
03 1Ningxia Qiyuan Pharmaceutical Co., Ltd. Yinchuan City CN
04 1Xi'an Lijun Pharmaceutical Co. Ltd Xi'an CN
01 4Tetracycline hydrochloride
02 1Tetracycline hydrochloride, Type 2
01 5China
01 2Expired
02 3Valid
Tetracycline Hydrochloride, Type 2
Certificate Number : CEP 2023-381 - Rev 00
Status : Valid
Issue Date : 2024-02-28
Type : Chemical
Substance Number : 210
Certificate Number : R0-CEP 2019-325 - Rev 00
Status : Valid
Issue Date : 2022-01-10
Type : Chemical
Substance Number : 210
Certificate Number : R1-CEP 2001-349 - Rev 04
Status : Valid
Issue Date : 2019-12-11
Type : Chemical
Substance Number : 210
Certificate Number : R0-CEP 2008-107 - Rev 00
Status : Expired
Issue Date : 2009-09-24
Type : Chemical
Substance Number : 210
Certificate Number : R0-CEP 2006-128 - Rev 01
Status : Expired
Issue Date : 2011-03-29
Type : Chemical
Substance Number : 210
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A Supramycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Supramycin, including repackagers and relabelers. The FDA regulates Supramycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Supramycin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Supramycin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Supramycin supplier is an individual or a company that provides Supramycin active pharmaceutical ingredient (API) or Supramycin finished formulations upon request. The Supramycin suppliers may include Supramycin API manufacturers, exporters, distributors and traders.
click here to find a list of Supramycin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Supramycin CEP of the European Pharmacopoeia monograph is often referred to as a Supramycin Certificate of Suitability (COS). The purpose of a Supramycin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Supramycin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Supramycin to their clients by showing that a Supramycin CEP has been issued for it. The manufacturer submits a Supramycin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Supramycin CEP holder for the record. Additionally, the data presented in the Supramycin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Supramycin DMF.
A Supramycin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Supramycin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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