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
01 5Ciprofloxacin
02 1Ciprofloxacin, Process II
01 1China
02 1Germany
03 1India
04 3Spain
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 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 2020-120 - Rev 04
Status : Valid
Issue Date : 2026-04-10
Type : Chemical
Substance Number : 1089
96
PharmaCompass offers a list of Ciprofloxacin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ciprofloxacin manufacturer or Ciprofloxacin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ciprofloxacin manufacturer or Ciprofloxacin supplier.
A Flociprin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flociprin, including repackagers and relabelers. The FDA regulates Flociprin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flociprin 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 Flociprin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Flociprin supplier is an individual or a company that provides Flociprin active pharmaceutical ingredient (API) or Flociprin finished formulations upon request. The Flociprin suppliers may include Flociprin API manufacturers, exporters, distributors and traders.
click here to find a list of Flociprin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Flociprin CEP of the European Pharmacopoeia monograph is often referred to as a Flociprin Certificate of Suitability (COS). The purpose of a Flociprin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Flociprin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Flociprin to their clients by showing that a Flociprin CEP has been issued for it. The manufacturer submits a Flociprin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Flociprin CEP holder for the record. Additionally, the data presented in the Flociprin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Flociprin DMF.
A Flociprin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Flociprin 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 Flociprin suppliers with CEP (COS) on PharmaCompass.
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