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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
Certificate Number : R1-CEP 2012-171 - Rev 01
Status : Valid
Issue Date : 2022-11-10
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
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 : 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
A CAS-64-75-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-64-75-5, including repackagers and relabelers. The FDA regulates CAS-64-75-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-64-75-5 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 CAS-64-75-5 supplier is an individual or a company that provides CAS-64-75-5 active pharmaceutical ingredient (API) or CAS-64-75-5 finished formulations upon request. The CAS-64-75-5 suppliers may include CAS-64-75-5 API manufacturers, exporters, distributors and traders.
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A CAS-64-75-5 CEP of the European Pharmacopoeia monograph is often referred to as a CAS-64-75-5 Certificate of Suitability (COS). The purpose of a CAS-64-75-5 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CAS-64-75-5 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CAS-64-75-5 to their clients by showing that a CAS-64-75-5 CEP has been issued for it. The manufacturer submits a CAS-64-75-5 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CAS-64-75-5 CEP holder for the record. Additionally, the data presented in the CAS-64-75-5 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CAS-64-75-5 DMF.
A CAS-64-75-5 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CAS-64-75-5 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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