Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1COHANCE LIFESCIENCES LIMITED Hyderabad IN
02 1AMSA S.P.A. - ANONIMA MATERIE SINTETICHE & AFFINI Como IT
03 1BIOINDUSTRIA L.I.M. S.P.A. Novi Ligure IT
04 1CLAROCHEM IRELAND LTD. Dublin 15 IE
05 1DAEHE BIOPHARMA CO., LTD. Siheung City KR
06 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
01 6Levodropropizine
01 2India
02 1Ireland
03 2Italy
04 1South Korea
01 1Expired
02 4Valid
03 1Withdrawn by Holder
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2023-110 - Rev 00
Status : Valid
Issue Date : 2024-05-24
Type : Chemical
Substance Number : 1535
Certificate Number : R1-CEP 2013-121 - Rev 00
Status : Valid
Issue Date : 2020-03-31
Type : Chemical
Substance Number : 1535
Certificate Number : R0-CEP 2013-156 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2018-03-07
Type : Chemical
Substance Number : 1535
Certificate Number : R1-CEP 2012-083 - Rev 01
Status : Valid
Issue Date : 2020-01-17
Type : Chemical
Substance Number : 1535
Certificate Number : R0-CEP 2012-401 - Rev 00
Status : Expired
Issue Date : 2014-04-24
Type : Chemical
Substance Number : 1535
Certificate Number : R1-CEP 2016-174 - Rev 00
Status : Valid
Issue Date : 2022-10-21
Type : Chemical
Substance Number : 1535
A Levodropropizine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levodropropizine, including repackagers and relabelers. The FDA regulates Levodropropizine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levodropropizine 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 Levodropropizine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levodropropizine supplier is an individual or a company that provides Levodropropizine active pharmaceutical ingredient (API) or Levodropropizine finished formulations upon request. The Levodropropizine suppliers may include Levodropropizine API manufacturers, exporters, distributors and traders.
click here to find a list of Levodropropizine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levodropropizine CEP of the European Pharmacopoeia monograph is often referred to as a Levodropropizine Certificate of Suitability (COS). The purpose of a Levodropropizine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Levodropropizine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Levodropropizine to their clients by showing that a Levodropropizine CEP has been issued for it. The manufacturer submits a Levodropropizine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Levodropropizine CEP holder for the record. Additionally, the data presented in the Levodropropizine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Levodropropizine DMF.
A Levodropropizine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Levodropropizine 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 Levodropropizine suppliers with CEP (COS) on PharmaCompass.
We have 6 companies offering Levodropropizine
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