01 1EDMOND PHARMA S.R.L. Paderno Dugnano IT
02 1Lusochimica S.p.A. Lomagna IT
01 2Carteolol hydrochloride
01 2Italy
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2005-199 - Rev 01
Status : Valid
Issue Date : 2022-10-10
Type : Chemical
Substance Number : 1972
Certificate Number : R1-CEP 2002-228 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2015-04-24
Type : Chemical
Substance Number : 1972
A (+/-)-Carteolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+/-)-Carteolol Hydrochloride, including repackagers and relabelers. The FDA regulates (+/-)-Carteolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+/-)-Carteolol 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 (+/-)-Carteolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+/-)-Carteolol Hydrochloride supplier is an individual or a company that provides (+/-)-Carteolol Hydrochloride active pharmaceutical ingredient (API) or (+/-)-Carteolol Hydrochloride finished formulations upon request. The (+/-)-Carteolol Hydrochloride suppliers may include (+/-)-Carteolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of (+/-)-Carteolol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (+/-)-Carteolol Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a (+/-)-Carteolol Hydrochloride Certificate of Suitability (COS). The purpose of a (+/-)-Carteolol Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of (+/-)-Carteolol Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of (+/-)-Carteolol Hydrochloride to their clients by showing that a (+/-)-Carteolol Hydrochloride CEP has been issued for it. The manufacturer submits a (+/-)-Carteolol Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a (+/-)-Carteolol Hydrochloride CEP holder for the record. Additionally, the data presented in the (+/-)-Carteolol Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the (+/-)-Carteolol Hydrochloride DMF.
A (+/-)-Carteolol Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. (+/-)-Carteolol Hydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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