01 1CHIFENG PHARMACEUTICAL CO., LTD. Chifeng CN
02 1HEBEI JIANMIN STARCH GLUCOSE CO., LTD. Ningjin CN
03 3Hebei Shengxue Dacheng Pharmaceutical Co., Ltd. Shijiazhuang City CN
04 1INNER MONGOLIA GLINT PHARMACEUTICAL CO., LTD. Chifeng CN
05 1JIANGXI GUOYAO PHARMACEUTICAL LIMITED LIABILITY COMPANY Nanchang CN
06 1Norbrook Laboratories LIMITED Newry IE
07 1SHANDONG JINYANG PHARMACEUTICAL CO., LTD. Zibo City CN
08 2YANCHENG DAFENG AREA TIANSHENG JOINT PHARMACEUTICAL CO., LTD Yancheng City CN
09 2YANGZHOU LIBERTY PHARMACEUTICAL CO., LTD. Yangzhou CN
01 10Oxytetracycline hydrochloride
02 1Oxytetracycline hydrochloride, For use in the manufacture of parenteral preparations
03 1Oxytetracycline hydrochloride, Process B - Micronised, non-micronised
04 1Oxytetracycline hydrochloride, Process II
01 12China
02 1United Kingdom
01 9Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 3Withdrawn by Holder
Oxytetracycline Hydrochloride, Process II
Certificate Number : CEP 2021-442 - Rev 01
Status : Valid
Issue Date : 2024-11-27
Type : Chemical
Substance Number : 198
Certificate Number : CEP 2002-070 - Rev 02
Status : Valid
Issue Date : 2025-01-02
Type : Chemical
Substance Number : 198
Oxytetracycline Hydrochloride, Process B - Micro...
Certificate Number : R1-CEP 2013-090 - Rev 02
Status : Valid
Issue Date : 2021-09-09
Type : Chemical
Substance Number : 198
Certificate Number : R0-CEP 2021-099 - Rev 01
Status : Valid
Issue Date : 2022-06-28
Type : Chemical
Substance Number : 198
Certificate Number : CEP 2021-412 - Rev 02
Status : Valid
Issue Date : 2025-01-16
Type : Chemical
Substance Number : 198
Certificate Number : R1-CEP 2001-125 - Rev 02
Status : Valid
Issue Date : 2018-08-14
Type : Chemical
Substance Number : 198
Certificate Number : R1-CEP 1999-162 - Rev 06
Status : Valid
Issue Date : 2017-04-19
Type : Chemical
Substance Number : 198
Certificate Number : R0-CEP 2008-165 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2010-05-12
Type : Chemical
Substance Number : 198
Certificate Number : R1-CEP 2010-080 - Rev 03
Status : Valid
Issue Date : 2019-05-09
Type : Chemical
Substance Number : 198
Oxytetracycline Hydrochloride, For Use In The Ma...
Certificate Number : CEP 2018-119 - Rev 04
Status : Valid
Issue Date : 2025-02-18
Type : Chemical
Substance Number : 198
14
PharmaCompass offers a list of Oxytetracycline Hydrochloride 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 Oxytetracycline Hydrochloride manufacturer or Oxytetracycline Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Oxytetracycline Hydrochloride API Price utilized in the formulation of products. Oxytetracycline Hydrochloride API Price is not always fixed or binding as the Oxytetracycline Hydrochloride Price is obtained through a variety of data sources. The Oxytetracycline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxyvet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxyvet, including repackagers and relabelers. The FDA regulates Oxyvet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxyvet 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 Oxyvet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxyvet supplier is an individual or a company that provides Oxyvet active pharmaceutical ingredient (API) or Oxyvet finished formulations upon request. The Oxyvet suppliers may include Oxyvet API manufacturers, exporters, distributors and traders.
click here to find a list of Oxyvet suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxyvet CEP of the European Pharmacopoeia monograph is often referred to as a Oxyvet Certificate of Suitability (COS). The purpose of a Oxyvet CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Oxyvet EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Oxyvet to their clients by showing that a Oxyvet CEP has been issued for it. The manufacturer submits a Oxyvet CEP (COS) as part of the market authorization procedure, and it takes on the role of a Oxyvet CEP holder for the record. Additionally, the data presented in the Oxyvet CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Oxyvet DMF.
A Oxyvet CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Oxyvet 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 Oxyvet suppliers with CEP (COS) on PharmaCompass.
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