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
A Actisite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Actisite, including repackagers and relabelers. The FDA regulates Actisite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Actisite 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 Actisite manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Actisite supplier is an individual or a company that provides Actisite active pharmaceutical ingredient (API) or Actisite finished formulations upon request. The Actisite suppliers may include Actisite API manufacturers, exporters, distributors and traders.
click here to find a list of Actisite suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Actisite CEP of the European Pharmacopoeia monograph is often referred to as a Actisite Certificate of Suitability (COS). The purpose of a Actisite CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Actisite EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Actisite to their clients by showing that a Actisite CEP has been issued for it. The manufacturer submits a Actisite CEP (COS) as part of the market authorization procedure, and it takes on the role of a Actisite CEP holder for the record. Additionally, the data presented in the Actisite CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Actisite DMF.
A Actisite CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Actisite 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 Actisite suppliers with CEP (COS) on PharmaCompass.
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