01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1AUROBINDO PHARMA LIMITED Hyderabad IN
03 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
04 1JANSSEN PHARMACEUTICA NV Beerse BE
05 1Janssen Pharmaceutical Ltd County Cork IE
06 2SRI KRISHNA PHARMACEUTICALS LIMITED Hyderabad IN
07 2VASUDHA PHARMA CHEM LIMITED Hyderabad IN
01 7Domperidone
02 2Domperidone, Process II
01 1Belgium
02 7India
03 1U.S.A
01 1Expired
02 6Valid
03 2Withdrawn by Holder
Certificate Number : CEP 2004-096 - Rev 05
Status : Valid
Issue Date : 2023-11-14
Type : Chemical
Substance Number : 1009
Certificate Number : R0-CEP 2003-031 - Rev 01
Status : Expired
Issue Date : 2004-10-01
Type : Chemical
Substance Number : 1009
Certificate Number : R1-CEP 1996-069 - Rev 10
Status : Valid
Issue Date : 2019-10-22
Type : Chemical
Substance Number : 1009
Certificate Number : R0-CEP 1999-129 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2003-07-03
Type : Chemical
Substance Number : 1009
Certificate Number : CEP 1997-094 - Rev 10
Status : Valid
Issue Date : 2024-12-20
Type : Chemical
Substance Number : 1009
Certificate Number : CEP 2022-374 - Rev 01
Status : Valid
Issue Date : 2024-12-20
Type : Chemical
Substance Number : 1009
Certificate Number : R0-CEP 2020-315 - Rev 01
Status : Valid
Issue Date : 2023-01-31
Type : Chemical
Substance Number : 1009
Certificate Number : R1-CEP 2007-203 - Rev 04
Status : Valid
Issue Date : 2020-09-03
Type : Chemical
Substance Number : 1009
Certificate Number : R1-CEP 2002-166 - Rev 04
Status : Withdrawn by Holder
Issue Date : 2015-10-08
Type : Chemical
Substance Number : 1009
A Ovaprim manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ovaprim, including repackagers and relabelers. The FDA regulates Ovaprim manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ovaprim 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 Ovaprim manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ovaprim supplier is an individual or a company that provides Ovaprim active pharmaceutical ingredient (API) or Ovaprim finished formulations upon request. The Ovaprim suppliers may include Ovaprim API manufacturers, exporters, distributors and traders.
click here to find a list of Ovaprim suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ovaprim CEP of the European Pharmacopoeia monograph is often referred to as a Ovaprim Certificate of Suitability (COS). The purpose of a Ovaprim CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ovaprim EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ovaprim to their clients by showing that a Ovaprim CEP has been issued for it. The manufacturer submits a Ovaprim CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ovaprim CEP holder for the record. Additionally, the data presented in the Ovaprim CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ovaprim DMF.
A Ovaprim CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ovaprim 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 Ovaprim suppliers with CEP (COS) on PharmaCompass.
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