Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1BAYER AG Leverkusen DE
03 2DIPHARMA FRANCIS S.R.L. Baranzate IT
04 1EVONIK OPERATIONS GMBH Essen DE
05 1F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT
06 1IPCA Laboratories Limited Mumbai IN
07 1PCAS (SELOC France Site) Limay FR
08 1SHILPA PHARMA LIFESCIENCES LIMITED Raichur IN
09 1SHOUGUANG FUKANG PHARMACEUTICAL CO., LTD. Shouguang City CN
10 1SIEGFRIED LTD. Zofingen CH
11 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
12 1Unique Chemicals (A Division of J.B. Chemicals & Pharmaceuticals Ltd.) Mumbai IN
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : CEP 1996-105 - Rev 05
Status : Valid
Issue Date : 2024-04-22
Type : Chemical
Substance Number : 627
27
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A Procardia XL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Procardia XL, including repackagers and relabelers. The FDA regulates Procardia XL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Procardia XL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Procardia XL supplier is an individual or a company that provides Procardia XL active pharmaceutical ingredient (API) or Procardia XL finished formulations upon request. The Procardia XL suppliers may include Procardia XL API manufacturers, exporters, distributors and traders.
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A Procardia XL CEP of the European Pharmacopoeia monograph is often referred to as a Procardia XL Certificate of Suitability (COS). The purpose of a Procardia XL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Procardia XL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Procardia XL to their clients by showing that a Procardia XL CEP has been issued for it. The manufacturer submits a Procardia XL CEP (COS) as part of the market authorization procedure, and it takes on the role of a Procardia XL CEP holder for the record. Additionally, the data presented in the Procardia XL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Procardia XL DMF.
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