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01 1BAYER AG Leverkusen DE
02 2QUIMICA SINTETICA S.A. Alcala De Henares ES
03 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
04 1Uquifa Mexico S.A. de C.V. Jiutepec MX
05 1ZHEJIANG GUOBANG PHARMACEUTICAL CO., LTD. Shaoxing CN
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01 5Ciprofloxacin
02 1Ciprofloxacin, Process II
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01 1China
02 1Germany
03 1India
04 3Spain
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01 6Valid
Certificate Number : R1-CEP 1998-102 - Rev 06
Status : Valid
Issue Date : 2017-03-06
Type : Chemical
Substance Number : 1089
Certificate Number : CEP 2004-199 - Rev 07
Status : Valid
Issue Date : 2023-12-06
Type : Chemical
Substance Number : 1089
Certificate Number : CEP 2021-219 - Rev 03
Status : Valid
Issue Date : 2024-10-30
Type : Chemical
Substance Number : 1089
Certificate Number : R1-CEP 2009-279 - Rev 02
Status : Valid
Issue Date : 2015-05-29
Type : Chemical
Substance Number : 1089
Certificate Number : CEP 2004-173 - Rev 01
Status : Valid
Issue Date : 2024-02-15
Type : Chemical
Substance Number : 1089
Certificate Number : CEP 2020-120 - Rev 03
Status : Valid
Issue Date : 2025-01-17
Type : Chemical
Substance Number : 1089
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PharmaCompass offers a list of Ciprofloxacin 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 Ciprofloxacin manufacturer or Ciprofloxacin supplier for your needs.
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A CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER, including repackagers and relabelers. The FDA regulates CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER 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 CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER supplier is an individual or a company that provides CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER active pharmaceutical ingredient (API) or CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER finished formulations upon request. The CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER suppliers may include CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER API manufacturers, exporters, distributors and traders.
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A CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER CEP of the European Pharmacopoeia monograph is often referred to as a CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER Certificate of Suitability (COS). The purpose of a CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER to their clients by showing that a CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER CEP has been issued for it. The manufacturer submits a CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER CEP (COS) as part of the market authorization procedure, and it takes on the role of a CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER CEP holder for the record. Additionally, the data presented in the CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER DMF.
A CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 5 companies offering CIPRO IN DEXTROSE 5% IN PLASTIC CONTAINER
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