Suanfarma, at the Core of a Better Life.
01 1CIPAN - COMPANHIA INDUSTRIAL PRODUTORA DE ANTIBIOTICOS, S.A. Castanheira Do Ribatejo PT
02 2Fujian Fukang Pharmaceutical Co., Ltd. Fuzhou City CN
03 1NORTH CHINA PHARMACEUTICAL GOODSTAR CO., LTD. Chengde CN
04 1Ningxia Qiyuan Pharmaceutical Co., Ltd. Yinchuan City CN
05 1Xi'an Lijun Pharmaceutical Co. Ltd Xi'an CN
01 5Tetracycline hydrochloride
02 1Tetracycline hydrochloride, Type 2
01 5China
02 1Spain
01 2Expired
02 4Valid
Suanfarma, at the Core of a Better Life.
Suanfarma, at the Core of a Better Life.
Certificate Number : R1-CEP 2012-171 - Rev 01
Status : Valid
Issue Date : 2022-11-10
Type : Chemical
Substance Number : 210
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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PharmaCompass offers a list of Tetracycline Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tetracycline Hydrochloride manufacturer or Tetracycline Hydrochloride supplier for your needs.
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A ALA TET manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALA TET, including repackagers and relabelers. The FDA regulates ALA TET manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALA TET API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A ALA TET supplier is an individual or a company that provides ALA TET active pharmaceutical ingredient (API) or ALA TET finished formulations upon request. The ALA TET suppliers may include ALA TET API manufacturers, exporters, distributors and traders.
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A ALA TET CEP of the European Pharmacopoeia monograph is often referred to as a ALA TET Certificate of Suitability (COS). The purpose of a ALA TET CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ALA TET EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ALA TET to their clients by showing that a ALA TET CEP has been issued for it. The manufacturer submits a ALA TET CEP (COS) as part of the market authorization procedure, and it takes on the role of a ALA TET CEP holder for the record. Additionally, the data presented in the ALA TET CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ALA TET DMF.
A ALA TET CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ALA TET CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of ALA TET suppliers with CEP (COS) on PharmaCompass.
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