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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 1RAKS PHARMA PVT. LTD. Visakhapatnam IN
06 1Ranbaxy Laboratories Limited Gurgaon IN
07 1SHANDONG GUOBANG PHARMACEUTICAL CO., LTD. Weifang CN
08 1Shanghai International Pharmaceutical Co., Ltd. Shanghai CN
09 1YANCHENG SUHAI PHARMACEUTICAL CO., LTD. Dafeng District, Yancheng City CN
10 1YANGZHOU LIBERTY PHARMACEUTICAL CO., LTD. Yangzhou CN
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01 10Doxycycline hyclate
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01 7China
02 2India
03 1Portugal
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01 6Valid
02 2Withdrawn by EDQM Failure to CEP procedure
03 2Withdrawn by Holder
Certificate Number : R1-CEP 2004-163 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2011-06-01
Type : Chemical
Substance Number : 272
Certificate Number : CEP 1996-066 - Rev 07
Status : Valid
Issue Date : 2024-07-18
Type : Chemical
Substance Number : 272
Certificate Number : R1-CEP 2001-038 - Rev 02
Status : Valid
Issue Date : 2015-03-19
Type : Chemical
Substance Number : 272
Certificate Number : R0-CEP 2003-225 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2005-04-15
Type : Chemical
Substance Number : 272
Certificate Number : R1-CEP 2014-175 - Rev 00
Status : Valid
Issue Date : 2022-02-10
Type : Chemical
Substance Number : 272
Certificate Number : CEP 2022-336 - Rev 00
Status : Valid
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 272
Certificate Number : R2-CEP 1992-018 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2004-02-19
Type : Chemical
Substance Number : 272
Certificate Number : R1-CEP 1997-002 - Rev 04
Status : Withdrawn by Holder
Issue Date : 2014-11-14
Type : Chemical
Substance Number : 272
Certificate Number : R1-CEP 1999-100 - Rev 05
Status : Valid
Issue Date : 2022-05-06
Type : Chemical
Substance Number : 272
Certificate Number : CEP 2000-165 - Rev 08
Status : Valid
Issue Date : 2025-02-04
Type : Chemical
Substance Number : 272
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PharmaCompass offers a list of Doxycycline Hyclate 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 Hyclate manufacturer or Doxycycline Hyclate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Doxycycline Hyclate manufacturer or Doxycycline Hyclate supplier.
PharmaCompass also assists you with knowing the Doxycycline Hyclate API Price utilized in the formulation of products. Doxycycline Hyclate API Price is not always fixed or binding as the Doxycycline Hyclate Price is obtained through a variety of data sources. The Doxycycline Hyclate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DOXTERIC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DOXTERIC, including repackagers and relabelers. The FDA regulates DOXTERIC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DOXTERIC 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 DOXTERIC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DOXTERIC supplier is an individual or a company that provides DOXTERIC active pharmaceutical ingredient (API) or DOXTERIC finished formulations upon request. The DOXTERIC suppliers may include DOXTERIC API manufacturers, exporters, distributors and traders.
click here to find a list of DOXTERIC suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DOXTERIC CEP of the European Pharmacopoeia monograph is often referred to as a DOXTERIC Certificate of Suitability (COS). The purpose of a DOXTERIC CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DOXTERIC EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DOXTERIC to their clients by showing that a DOXTERIC CEP has been issued for it. The manufacturer submits a DOXTERIC CEP (COS) as part of the market authorization procedure, and it takes on the role of a DOXTERIC CEP holder for the record. Additionally, the data presented in the DOXTERIC CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DOXTERIC DMF.
A DOXTERIC CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DOXTERIC 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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