Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1CAMBREX KARLSKOGA AB Karlskoga SE
03 1DISHMAN CARBOGEN AMCIS LIMITED Ahmedabad IN
04 1EXCELLA GMBH & CO. KG Feucht DE
05 1Medigraph Pharmaceuticals Pvt. Ltd Taloja IN
06 1S.I.M.S. S.R.L. Reggello IT
07 1SIEGFRIED EVIONNAZ SA Evionnaz CH
01 7Bupivacaine hydrochloride
01 1Germany
02 2India
03 1Italy
04 1Spain
05 1Switzerland
06 1U.S.A
01 6Valid
02 1Withdrawn by Holder
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : R1-CEP 2010-277 - Rev 03
Status : Valid
Issue Date : 2022-01-24
Type : Chemical
Substance Number : 541
Certificate Number : R1-CEP 2011-254 - Rev 00
Status : Valid
Issue Date : 2019-01-31
Type : Chemical
Substance Number : 541
Certificate Number : R1-CEP 2009-038 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2017-07-28
Type : Chemical
Substance Number : 541
Certificate Number : CEP 2003-173 - Rev 04
Status : Valid
Issue Date : 2023-10-04
Type : Chemical
Substance Number : 541
Certificate Number : R1-CEP 2007-116 - Rev 02
Status : Valid
Issue Date : 2020-09-25
Type : Chemical
Substance Number : 541
Certificate Number : R1-CEP 2004-043 - Rev 04
Status : Valid
Issue Date : 2021-12-10
Type : Chemical
Substance Number : 541
Certificate Number : R1-CEP 2001-013 - Rev 02
Status : Valid
Issue Date : 2015-02-09
Type : Chemical
Substance Number : 541
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PharmaCompass offers a list of Bupivacaine Hydrochloride 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 Bupivacaine Hydrochloride manufacturer or Bupivacaine Hydrochloride supplier for your needs.
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A AH 2250 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AH 2250, including repackagers and relabelers. The FDA regulates AH 2250 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AH 2250 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 AH 2250 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AH 2250 supplier is an individual or a company that provides AH 2250 active pharmaceutical ingredient (API) or AH 2250 finished formulations upon request. The AH 2250 suppliers may include AH 2250 API manufacturers, exporters, distributors and traders.
click here to find a list of AH 2250 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AH 2250 CEP of the European Pharmacopoeia monograph is often referred to as a AH 2250 Certificate of Suitability (COS). The purpose of a AH 2250 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AH 2250 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AH 2250 to their clients by showing that a AH 2250 CEP has been issued for it. The manufacturer submits a AH 2250 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AH 2250 CEP holder for the record. Additionally, the data presented in the AH 2250 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AH 2250 DMF.
A AH 2250 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AH 2250 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 AH 2250 suppliers with CEP (COS) on PharmaCompass.
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