01 2CHIFENG PHARMACEUTICAL CO., LTD. Chifeng CN
02 2HEBEI JIANMIN STARCH GLUCOSE CO., LTD. Ningjin CN
03 3Hebei Shengxue Dacheng Pharmaceutical Co., Ltd. Shijiazhuang City CN
04 1Huashu Pharmaceutical Corporation Shijiazhuang CN
05 1INNER MONGOLIA HUASHU BIOLOGICAL TECHNOLOGY CO.LTD Tongliao City CN
06 2KRKA, d.d., Novo mesto Novo mesto SI
07 1Norbrook Laboratories LIMITED Newry IE
08 1SHANDONG JINYANG PHARMACEUTICAL CO., LTD. Zibo City CN
09 3YANGZHOU LIBERTY PHARMACEUTICAL CO., LTD. Yangzhou CN
01 11Oxytetracycline dihydrate
02 3Oxytetracycline dihydrate, Process B
03 1Oxytetracycline dihydrate, Process II
04 1Oxytetracycline dihydrate, Site B
01 13China
02 2Slovenia
03 1United Kingdom
01 10Valid
02 3Withdrawn by EDQM Failure to CEP procedure
03 3Withdrawn by Holder
Certificate Number : R0-CEP 2021-031 - Rev 00
Status : Valid
Issue Date : 2022-06-23
Type : Chemical
Substance Number : 199
Oxytetracycline Dihydrate, Process B
Certificate Number : CEP 2017-258 - Rev 01
Status : Valid
Issue Date : 2024-05-22
Type : Chemical
Substance Number : 199
Certificate Number : CEP 2004-055 - Rev 03
Status : Valid
Issue Date : 2024-10-09
Type : Chemical
Substance Number : 199
Certificate Number : R0-CEP 2018-238 - Rev 00
Status : Valid
Issue Date : 2020-01-17
Type : Chemical
Substance Number : 199
Certificate Number : R1-CEP 1997-127 - Rev 06
Status : Valid
Issue Date : 2017-04-19
Type : Chemical
Substance Number : 199
Certificate Number : R1-CEP 2002-035 - Rev 03
Status : Valid
Issue Date : 2023-03-13
Type : Chemical
Substance Number : 199
Oxytetracycline Dihydrate, Process B
Certificate Number : R1-CEP 2009-053 - Rev 02
Status : Valid
Issue Date : 2023-03-13
Type : Chemical
Substance Number : 199
Certificate Number : R1-CEP 2017-105 - Rev 00
Status : Valid
Issue Date : 2023-03-15
Type : Chemical
Substance Number : 199
Oxytetracycline Dihydrate, Process II
Certificate Number : CEP 2018-291 - Rev 02
Status : Valid
Issue Date : 2025-02-18
Type : Chemical
Substance Number : 199
Oxytetracycline Dihydrate, Site B
Certificate Number : R0-CEP 2023-054 - Rev 00
Status : Valid
Issue Date : 2023-05-26
Type : Chemical
Substance Number : 199
52
PharmaCompass offers a list of Oxytetracycline Dihydrate 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 Dihydrate manufacturer or Oxytetracycline Dihydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxytetracycline Dihydrate manufacturer or Oxytetracycline Dihydrate supplier.
PharmaCompass also assists you with knowing the Oxytetracycline Dihydrate API Price utilized in the formulation of products. Oxytetracycline Dihydrate API Price is not always fixed or binding as the Oxytetracycline Dihydrate Price is obtained through a variety of data sources. The Oxytetracycline Dihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tetran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetran, including repackagers and relabelers. The FDA regulates Tetran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetran 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 Tetran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetran supplier is an individual or a company that provides Tetran active pharmaceutical ingredient (API) or Tetran finished formulations upon request. The Tetran suppliers may include Tetran API manufacturers, exporters, distributors and traders.
click here to find a list of Tetran suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tetran CEP of the European Pharmacopoeia monograph is often referred to as a Tetran Certificate of Suitability (COS). The purpose of a Tetran CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tetran EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tetran to their clients by showing that a Tetran CEP has been issued for it. The manufacturer submits a Tetran CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tetran CEP holder for the record. Additionally, the data presented in the Tetran CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tetran DMF.
A Tetran CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tetran 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 Tetran suppliers with CEP (COS) on PharmaCompass.
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