Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak A.S. Olomouc CZ
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1CIPLA LIMITED Mumbai IN
04 1EXCELLA GMBH & CO. KG Feucht DE
05 1GLENMARK PHARMACEUTICALS LIMITED Mumbai IN
06 1MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
07 1SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. Linyi CN
08 1Unichem Laboratories Limited Mumbai IN
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Certificate Number : R1-CEP 2003-098 - Rev 02
Status : Valid
Issue Date : 2021-08-18
Type : Chemical
Substance Number : 1287
51
PharmaCompass offers a list of Alfuzosin HCl 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 Alfuzosin HCl manufacturer or Alfuzosin HCl supplier for your needs.
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A Xatral XL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xatral XL, including repackagers and relabelers. The FDA regulates Xatral XL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xatral 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 Xatral XL supplier is an individual or a company that provides Xatral XL active pharmaceutical ingredient (API) or Xatral XL finished formulations upon request. The Xatral XL suppliers may include Xatral XL API manufacturers, exporters, distributors and traders.
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A Xatral XL CEP of the European Pharmacopoeia monograph is often referred to as a Xatral XL Certificate of Suitability (COS). The purpose of a Xatral XL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Xatral XL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Xatral XL to their clients by showing that a Xatral XL CEP has been issued for it. The manufacturer submits a Xatral XL CEP (COS) as part of the market authorization procedure, and it takes on the role of a Xatral XL CEP holder for the record. Additionally, the data presented in the Xatral XL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Xatral XL DMF.
A Xatral XL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Xatral XL 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 Xatral XL suppliers with CEP (COS) on PharmaCompass.
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