01 1CIPLA LIMITED Mumbai IN
02 2KRKA TOVARNA ZDRAVIL D.D. NOVO MESTO Novo mesto SI
03 1KRKA, d.d., Novo mesto Novo mesto SI
04 1NAKODA CHEMICALS LIMITED Hyderabad IN
05 1Smruthi Organics Limited Solapur IN
06 1ZHEJIANG LEPU PHARMACEUTICAL CO., LTD Taizhou City CN
01 5Norfloxacin
02 1Norfloxacin, Product code 312008
03 1Norfloxacin, Product code 312025
01 1China
02 3India
03 3Slovenia
01 4Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 2Withdrawn by Holder
Certificate Number : R1-CEP 2001-375 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2014-07-28
Type : Chemical
Substance Number : 1248
Norfloxacin, Product Code 312008
Certificate Number : CEP 2021-140 - Rev 02
Status : Valid
Issue Date : 2025-03-17
Type : Chemical
Substance Number : 1248
Norfloxacin, Product Code 312025
Certificate Number : CEP 2021-141 - Rev 02
Status : Valid
Issue Date : 2025-03-17
Type : Chemical
Substance Number : 1248
Certificate Number : R1-CEP 2000-270 - Rev 04
Status : Withdrawn by Holder
Issue Date : 2013-03-14
Type : Chemical
Substance Number : 1248
Certificate Number : CEP 2017-206 - Rev 02
Status : Valid
Issue Date : 2024-01-17
Type : Chemical
Substance Number : 1248
Certificate Number : R1-CEP 2001-409 - Rev 02
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2010-04-01
Type : Chemical
Substance Number : 1248
Certificate Number : CEP 2006-037 - Rev 05
Status : Valid
Issue Date : 2025-06-19
Type : Chemical
Substance Number : 1248
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PharmaCompass offers a list of Norfloxacin 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 Norfloxacin manufacturer or Norfloxacin supplier for your needs.
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A MolPort-001-738-625 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-738-625, including repackagers and relabelers. The FDA regulates MolPort-001-738-625 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-738-625 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 MolPort-001-738-625 supplier is an individual or a company that provides MolPort-001-738-625 active pharmaceutical ingredient (API) or MolPort-001-738-625 finished formulations upon request. The MolPort-001-738-625 suppliers may include MolPort-001-738-625 API manufacturers, exporters, distributors and traders.
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A MolPort-001-738-625 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-738-625 Certificate of Suitability (COS). The purpose of a MolPort-001-738-625 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-738-625 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-738-625 to their clients by showing that a MolPort-001-738-625 CEP has been issued for it. The manufacturer submits a MolPort-001-738-625 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-738-625 CEP holder for the record. Additionally, the data presented in the MolPort-001-738-625 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-738-625 DMF.
A MolPort-001-738-625 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-738-625 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 MolPort-001-738-625 suppliers with CEP (COS) on PharmaCompass.
We have 5 companies offering MolPort-001-738-625
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