PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
01 1ISOCHEM Vert Le Petit FR
02 1AMDIPHARM LIMITED Dublin IE
03 1Calao s.r.l. Milano IT
04 1FRESENIUS KABI ONCOLOGY LIMITED Kalyani IN
05 1SHILPA MEDICARE LIMITED Raichur IN
01 5Buflomedil Hydrochloride
01 1France
02 2India
03 1U.S.A
04 1United Kingdom
01 1Expired
02 1Valid
03 3Withdrawn by Holder
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
Certificate Number : R1-CEP 2003-201 - Rev 01
Status : Valid
Issue Date : 2011-02-08
Type : Chemical
Substance Number : 1398
Certificate Number : R0-CEP 2006-207 - Rev 02
Status : Expired
Issue Date : 2011-06-07
Type : Chemical
Substance Number : 1398
Certificate Number : R1-CEP 2000-131 - Rev 04
Status : Withdrawn by Holder
Issue Date : 2011-02-24
Type : Chemical
Substance Number : 1398
Certificate Number : R0-CEP 2010-346 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2013-04-04
Type : Chemical
Substance Number : 1398
Certificate Number : R0-CEP 2006-080 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2011-01-14
Type : Chemical
Substance Number : 1398
A Buflomedil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buflomedil, including repackagers and relabelers. The FDA regulates Buflomedil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buflomedil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Buflomedil supplier is an individual or a company that provides Buflomedil active pharmaceutical ingredient (API) or Buflomedil finished formulations upon request. The Buflomedil suppliers may include Buflomedil API manufacturers, exporters, distributors and traders.
click here to find a list of Buflomedil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Buflomedil CEP of the European Pharmacopoeia monograph is often referred to as a Buflomedil Certificate of Suitability (COS). The purpose of a Buflomedil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Buflomedil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Buflomedil to their clients by showing that a Buflomedil CEP has been issued for it. The manufacturer submits a Buflomedil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Buflomedil CEP holder for the record. Additionally, the data presented in the Buflomedil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Buflomedil DMF.
A Buflomedil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Buflomedil 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 Buflomedil suppliers with CEP (COS) on PharmaCompass.
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