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Status : Withdrawn by Holder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
A Bupivacaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bupivacaine Hydrochloride, including repackagers and relabelers. The FDA regulates Bupivacaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bupivacaine Hydrochloride 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 Bupivacaine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bupivacaine Hydrochloride supplier is an individual or a company that provides Bupivacaine Hydrochloride active pharmaceutical ingredient (API) or Bupivacaine Hydrochloride finished formulations upon request. The Bupivacaine Hydrochloride suppliers may include Bupivacaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Bupivacaine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bupivacaine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Bupivacaine Hydrochloride Certificate of Suitability (COS). The purpose of a Bupivacaine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Bupivacaine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Bupivacaine Hydrochloride to their clients by showing that a Bupivacaine Hydrochloride CEP has been issued for it. The manufacturer submits a Bupivacaine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Bupivacaine Hydrochloride CEP holder for the record. Additionally, the data presented in the Bupivacaine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Bupivacaine Hydrochloride DMF.
A Bupivacaine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Bupivacaine Hydrochloride 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 Bupivacaine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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