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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
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01 8Doxycycline monohydrate
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01 6China
02 1India
03 1Portugal
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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Status : Withdrawn by Holder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Status : Withdrawn by EDQM Failure to CEP pro...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 1996-064 - Rev 04
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2007-06-01
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Status : Withdrawn by Holder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 : 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
79
PharmaCompass offers a list of Doxycycline API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Doxycycline manufacturer or Doxycycline supplier for your needs.
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A Vibra Tabs manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vibra Tabs, including repackagers and relabelers. The FDA regulates Vibra Tabs manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vibra Tabs 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 Vibra Tabs supplier is an individual or a company that provides Vibra Tabs active pharmaceutical ingredient (API) or Vibra Tabs finished formulations upon request. The Vibra Tabs suppliers may include Vibra Tabs API manufacturers, exporters, distributors and traders.
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A Vibra Tabs CEP of the European Pharmacopoeia monograph is often referred to as a Vibra Tabs Certificate of Suitability (COS). The purpose of a Vibra Tabs CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vibra Tabs EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vibra Tabs to their clients by showing that a Vibra Tabs CEP has been issued for it. The manufacturer submits a Vibra Tabs CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vibra Tabs CEP holder for the record. Additionally, the data presented in the Vibra Tabs CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vibra Tabs DMF.
A Vibra Tabs CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vibra Tabs 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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