Suanfarma, at the Core of a Better Life.
01 1CIPAN - COMPANHIA INDUSTRIAL PRODUTORA DE ANTIBIOTICOS, S.A. Castanheira Do Ribatejo PT
02 1CURIA ITALY S.R.L. Origgio IT
03 2HOVIONE FARMACIENCIA S.A. Loures PT
04 1NIPPON KAYAKU CO., LTD. Chiyoda-Ku JP
05 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
06 1ZHEJIANG MEDICINE CO., LTD. Shaoxing CN
01 5Minocycline hydrochloride dihydrate
02 1Minocycline hydrochloride dihydrate, Grade B
03 1Minocycline hydrochloride dihydrate, Micronised
01 1China
02 1Japan
03 2Portugal
04 2Spain
05 1U.S.A
01 6Valid
02 1Withdrawn by Holder
Suanfarma, at the Core of a Better Life.
Suanfarma, at the Core of a Better Life.
Minocycline Hydrochloride Dihydrate
Certificate Number : R1-CEP 1999-002 - Rev 06
Status : Valid
Issue Date : 2022-12-02
Type : Chemical
Substance Number : 1030
Minocycline Hydrochloride Dihydrate
Certificate Number : CEP 2000-107 - Rev 10
Status : Valid
Issue Date : 2024-02-27
Type : Chemical
Substance Number : 1030
Minocycline Hydrochloride Dihydrate, Micronised
Certificate Number : R0-CEP 2022-299 - Rev 00
Status : Valid
Issue Date : 2022-10-11
Type : Chemical
Substance Number : 1030
Minocycline Hydrochloride Dihydrate, Grade B
Certificate Number : CEP 1997-078 - Rev 09
Status : Valid
Issue Date : 2024-07-17
Type : Chemical
Substance Number : 1030
Minocycline Hydrochloride Dihydrate
Certificate Number : R0-CEP 1999-072 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2004-08-20
Type : Chemical
Substance Number : 1030
Minocycline Hydrochloride Dihydrate
Certificate Number : R1-CEP 1998-152 - Rev 02
Status : Valid
Issue Date : 2009-12-11
Type : Chemical
Substance Number : 1030
Minocycline Hydrochloride Dihydrate
Certificate Number : CEP 2022-195 - Rev 00
Status : Valid
Issue Date : 2025-01-30
Type : Chemical
Substance Number : 1030
100
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A XIMINO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of XIMINO, including repackagers and relabelers. The FDA regulates XIMINO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. XIMINO 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 XIMINO supplier is an individual or a company that provides XIMINO active pharmaceutical ingredient (API) or XIMINO finished formulations upon request. The XIMINO suppliers may include XIMINO API manufacturers, exporters, distributors and traders.
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A XIMINO CEP of the European Pharmacopoeia monograph is often referred to as a XIMINO Certificate of Suitability (COS). The purpose of a XIMINO CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of XIMINO EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of XIMINO to their clients by showing that a XIMINO CEP has been issued for it. The manufacturer submits a XIMINO CEP (COS) as part of the market authorization procedure, and it takes on the role of a XIMINO CEP holder for the record. Additionally, the data presented in the XIMINO CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the XIMINO DMF.
A XIMINO CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. XIMINO 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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