01 1CAMBREX CHARLES CITY, INC. Charles City US
02 1Calao s.r.l. Milano IT
03 1DAIICHI SANKYO CO., LTD. Tokyo JP
04 1QUIMICA SINTETICA S.A. Alcala De Henares ES
05 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
06 2ZHEJIANG APELOA KANGYU PHARMACEUTICAL CO., LTD. Hengdian CN
01 6Ofloxacin
02 1Ofloxacin, Process H
01 2China
02 1India
03 1Japan
04 1Spain
05 2U.S.A
01 1Expired
02 4Valid
03 2Withdrawn by Holder
Certificate Number : R0-CEP 2001-436 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2005-03-24
Type : Chemical
Substance Number : 1455
Certificate Number : R0-CEP 2002-029 - Rev 01
Status : Expired
Issue Date : 2004-10-13
Type : Chemical
Substance Number : 1455
Certificate Number : CEP 2003-210 - Rev 04
Status : Valid
Issue Date : 2024-12-20
Type : Chemical
Substance Number : 1455
Certificate Number : CEP 2000-134 - Rev 07
Status : Valid
Issue Date : 2023-10-11
Type : Chemical
Substance Number : 1455
Certificate Number : CEP 2000-106 - Rev 10
Status : Valid
Issue Date : 2025-02-17
Type : Chemical
Substance Number : 1455
Certificate Number : CEP 2021-213 - Rev 01
Status : Valid
Issue Date : 2023-10-06
Type : Chemical
Substance Number : 1455
Certificate Number : R1-CEP 2002-146 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2011-02-07
Type : Chemical
Substance Number : 1455
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PharmaCompass offers a list of Ofloxacin 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 Ofloxacin manufacturer or Ofloxacin supplier for your needs.
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PharmaCompass also assists you with knowing the Ofloxacin API Price utilized in the formulation of products. Ofloxacin API Price is not always fixed or binding as the Ofloxacin Price is obtained through a variety of data sources. The Ofloxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A H778 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of H778, including repackagers and relabelers. The FDA regulates H778 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. H778 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 H778 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A H778 supplier is an individual or a company that provides H778 active pharmaceutical ingredient (API) or H778 finished formulations upon request. The H778 suppliers may include H778 API manufacturers, exporters, distributors and traders.
click here to find a list of H778 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A H778 CEP of the European Pharmacopoeia monograph is often referred to as a H778 Certificate of Suitability (COS). The purpose of a H778 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of H778 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of H778 to their clients by showing that a H778 CEP has been issued for it. The manufacturer submits a H778 CEP (COS) as part of the market authorization procedure, and it takes on the role of a H778 CEP holder for the record. Additionally, the data presented in the H778 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the H778 DMF.
A H778 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. H778 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 H778 suppliers with CEP (COS) on PharmaCompass.
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