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
01 4Minocycline hydrochloride dihydrate
02 1Minocycline hydrochloride dihydrate, Grade B
03 1Minocycline hydrochloride dihydrate, Micronised
01 1Japan
02 2Portugal
03 2Spain
04 1U.S.A
01 5Valid
02 1Withdrawn by Holder
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Status : Withdrawn by Holder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
A Minocycline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Minocycline, including repackagers and relabelers. The FDA regulates Minocycline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Minocycline 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 Minocycline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Minocycline supplier is an individual or a company that provides Minocycline active pharmaceutical ingredient (API) or Minocycline finished formulations upon request. The Minocycline suppliers may include Minocycline API manufacturers, exporters, distributors and traders.
click here to find a list of Minocycline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Minocycline CEP of the European Pharmacopoeia monograph is often referred to as a Minocycline Certificate of Suitability (COS). The purpose of a Minocycline CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Minocycline EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Minocycline to their clients by showing that a Minocycline CEP has been issued for it. The manufacturer submits a Minocycline CEP (COS) as part of the market authorization procedure, and it takes on the role of a Minocycline CEP holder for the record. Additionally, the data presented in the Minocycline CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Minocycline DMF.
A Minocycline CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Minocycline 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 Minocycline suppliers with CEP (COS) on PharmaCompass.
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