01 1Hebei Dongfeng Pharmaceutical Co., Ltd Handan City CN
02 1Hovione PharmaScience Limited Taipa MO
03 1KAIFENG PHARMACEUTICAL (GROUP) CO., LTD. Kaifeng CN
04 1KUNSHAN CHEMICAL AND PHARMACEUTICAL FACTORY Kunshan City CN
05 1Ranbaxy Laboratories Limited Gurgaon IN
06 1Shanghai International Pharmaceutical Co., Ltd. Shanghai CN
07 1YANCHENG SUHAI PHARMACEUTICAL CO., LTD. Dafeng District, Yancheng City CN
08 1YANGZHOU LIBERTY PHARMACEUTICAL CO., LTD. Yangzhou CN
01 8Doxycycline monohydrate
01 6China
02 1India
03 1Portugal
01 4Valid
02 2Withdrawn by EDQM Failure to CEP procedure
03 2Withdrawn by Holder
Certificate Number : R1-CEP 2004-162 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2011-06-01
Type : Chemical
Substance Number : 820
Certificate Number : R1-CEP 1997-115 - Rev 07
Status : Valid
Issue Date : 2021-09-10
Type : Chemical
Substance Number : 820
Certificate Number : R1-CEP 2012-243 - Rev 00
Status : Valid
Issue Date : 2019-01-28
Type : Chemical
Substance Number : 820
Certificate Number : R0-CEP 2003-226 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2005-04-27
Type : Chemical
Substance Number : 820
Certificate Number : R1-CEP 1997-072 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2008-03-17
Type : Chemical
Substance Number : 820
Certificate Number : R1-CEP 1996-064 - Rev 04
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2007-06-01
Type : Chemical
Substance Number : 820
Certificate Number : CEP 1999-157 - Rev 05
Status : Valid
Issue Date : 2024-03-06
Type : Chemical
Substance Number : 820
Certificate Number : R1-CEP 2013-052 - Rev 00
Status : Valid
Issue Date : 2019-02-12
Type : Chemical
Substance Number : 820
A Doxycycline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxycycline, including repackagers and relabelers. The FDA regulates Doxycycline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxycycline 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 Doxycycline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Doxycycline supplier is an individual or a company that provides Doxycycline active pharmaceutical ingredient (API) or Doxycycline finished formulations upon request. The Doxycycline suppliers may include Doxycycline API manufacturers, exporters, distributors and traders.
click here to find a list of Doxycycline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Doxycycline CEP of the European Pharmacopoeia monograph is often referred to as a Doxycycline Certificate of Suitability (COS). The purpose of a Doxycycline CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Doxycycline EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Doxycycline to their clients by showing that a Doxycycline CEP has been issued for it. The manufacturer submits a Doxycycline CEP (COS) as part of the market authorization procedure, and it takes on the role of a Doxycycline CEP holder for the record. Additionally, the data presented in the Doxycycline CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Doxycycline DMF.
A Doxycycline CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Doxycycline 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 Doxycycline suppliers with CEP (COS) on PharmaCompass.
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