01 1BAYER AG Leverkusen DE
02 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
03 1NEULAND LABORATORIES LIMITED Hyderabad IN
04 2QUIMICA SINTETICA S.A. Alcala De Henares ES
05 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
06 1Uquifa Mexico S.A. de C.V. Jiutepec MX
07 1ZHEJIANG GUOBANG PHARMACEUTICAL CO., LTD. Shaoxing CN
01 7Ciprofloxacin
02 1Ciprofloxacin, Process II
01 1China
02 2Gabon
03 1Germany
04 1India
05 3Spain
01 8Valid
Certificate Number : R1-CEP 1998-102 - Rev 06
Status : Valid
Issue Date : 2017-03-06
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 : CEP 2004-199 - Rev 07
Status : Valid
Issue Date : 2023-12-06
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 2011-389 - Rev 04
Status : Valid
Issue Date : 2025-01-13
Type : Chemical
Substance Number : 1089
Certificate Number : CEP 2005-133 - Rev 04
Status : Valid
Issue Date : 2024-11-04
Type : Chemical
Substance Number : 1089
Certificate Number : CEP 2020-120 - Rev 03
Status : Valid
Issue Date : 2025-01-17
Type : Chemical
Substance Number : 1089
34
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 Proksi 500 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Proksi 500, including repackagers and relabelers. The FDA regulates Proksi 500 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Proksi 500 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 Proksi 500 supplier is an individual or a company that provides Proksi 500 active pharmaceutical ingredient (API) or Proksi 500 finished formulations upon request. The Proksi 500 suppliers may include Proksi 500 API manufacturers, exporters, distributors and traders.
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A Proksi 500 CEP of the European Pharmacopoeia monograph is often referred to as a Proksi 500 Certificate of Suitability (COS). The purpose of a Proksi 500 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Proksi 500 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Proksi 500 to their clients by showing that a Proksi 500 CEP has been issued for it. The manufacturer submits a Proksi 500 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Proksi 500 CEP holder for the record. Additionally, the data presented in the Proksi 500 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Proksi 500 DMF.
A Proksi 500 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Proksi 500 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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