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
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 : R0-CEP 2021-031 - Rev 00
Status : Valid
Issue Date : 2022-06-23
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 : CEP 2018-238 - Rev 01
Status : Valid
Issue Date : 2025-08-13
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
16
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 E703 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E703, including repackagers and relabelers. The FDA regulates E703 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E703 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 E703 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E703 supplier is an individual or a company that provides E703 active pharmaceutical ingredient (API) or E703 finished formulations upon request. The E703 suppliers may include E703 API manufacturers, exporters, distributors and traders.
click here to find a list of E703 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A E703 CEP of the European Pharmacopoeia monograph is often referred to as a E703 Certificate of Suitability (COS). The purpose of a E703 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of E703 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of E703 to their clients by showing that a E703 CEP has been issued for it. The manufacturer submits a E703 CEP (COS) as part of the market authorization procedure, and it takes on the role of a E703 CEP holder for the record. Additionally, the data presented in the E703 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the E703 DMF.
A E703 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. E703 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 E703 suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering E703
Get in contact with the supplier of your choice:
