01 1CHEMI S.P.A. Patrica IT
02 1DIVI'S LABORATORIES LIMITED Hyderabad IN
03 1IPCA Laboratories Limited Mumbai IN
04 1MYLAN LABORATORIES LIMITED Hyderabad IN
05 1TAPI NL B.V. Amsterdam NL
01 4Nabumetone
02 1Nabumetone, FV 4074
01 2India
02 1Italy
03 1U.S.A
04 1Blank
01 3Valid
02 2Withdrawn by Holder
Certificate Number : R1-CEP 2007-002 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2014-03-10
Type : Chemical
Substance Number : 1350
Certificate Number : R1-CEP 1999-055 - Rev 06
Status : Valid
Issue Date : 2018-08-23
Type : Chemical
Substance Number : 1350
Certificate Number : R1-CEP 2004-078 - Rev 02
Status : Valid
Issue Date : 2017-02-23
Type : Chemical
Substance Number : 1350
Certificate Number : R1-CEP 2006-092 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2017-09-25
Type : Chemical
Substance Number : 1350
Portfolio PDF
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Certificate Number : CEP 2000-115 - Rev 13
Status : Valid
Issue Date : 2025-03-12
Type : Chemical
Substance Number : 1350
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Nabumetone 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 Nabumetone manufacturer or Nabumetone supplier for your needs.
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PharmaCompass also assists you with knowing the Nabumetone API Price utilized in the formulation of products. Nabumetone API Price is not always fixed or binding as the Nabumetone Price is obtained through a variety of data sources. The Nabumetone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Relifen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Relifen, including repackagers and relabelers. The FDA regulates Relifen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Relifen 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 Relifen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Relifen supplier is an individual or a company that provides Relifen active pharmaceutical ingredient (API) or Relifen finished formulations upon request. The Relifen suppliers may include Relifen API manufacturers, exporters, distributors and traders.
click here to find a list of Relifen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Relifen CEP of the European Pharmacopoeia monograph is often referred to as a Relifen Certificate of Suitability (COS). The purpose of a Relifen CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Relifen EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Relifen to their clients by showing that a Relifen CEP has been issued for it. The manufacturer submits a Relifen CEP (COS) as part of the market authorization procedure, and it takes on the role of a Relifen CEP holder for the record. Additionally, the data presented in the Relifen CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Relifen DMF.
A Relifen CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Relifen 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 Relifen suppliers with CEP (COS) on PharmaCompass.
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