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01 1FRANCOPIA Paris FR
02 1MACFARLAN SMITH LIMITED Edinburgh GB
03 1RUSAN PHARMA LTD Mumbai IN
01 3Apomorphine hydrochloride hemihydrate
01 1France
02 1India
03 1United Kingdom
01 3Valid
Apomorphine Hydrochloride Hemihydrate
Certificate Number : CEP 2008-332 - Rev 04
Status : Valid
Issue Date : 2024-03-01
Type : Chemical
Substance Number : 136
Apomorphine Hydrochloride Hemihydrate
Certificate Number : R1-CEP 2006-237 - Rev 03
Status : Valid
Issue Date : 2020-12-16
Type : Chemical
Substance Number : 136
Apomorphine Hydrochloride Hemihydrate
Certificate Number : CEP 2021-135 - Rev 00
Status : Valid
Issue Date : 2024-02-14
Type : Chemical
Substance Number : 136
A Apomorphine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Apomorphine Hydrochloride, including repackagers and relabelers. The FDA regulates Apomorphine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Apomorphine 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 Apomorphine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Apomorphine Hydrochloride supplier is an individual or a company that provides Apomorphine Hydrochloride active pharmaceutical ingredient (API) or Apomorphine Hydrochloride finished formulations upon request. The Apomorphine Hydrochloride suppliers may include Apomorphine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Apomorphine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Apomorphine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Apomorphine Hydrochloride Certificate of Suitability (COS). The purpose of a Apomorphine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Apomorphine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Apomorphine Hydrochloride to their clients by showing that a Apomorphine Hydrochloride CEP has been issued for it. The manufacturer submits a Apomorphine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Apomorphine Hydrochloride CEP holder for the record. Additionally, the data presented in the Apomorphine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Apomorphine Hydrochloride DMF.
A Apomorphine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Apomorphine 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 Apomorphine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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