Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
02 1AGC PHARMA CHEMICALS EUROPE S.L.U. Malgrat De Mar ES
03 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
04 1HETERO DRUGS LIMITED Hyderabad IN
01 4Mexiletine hydrochloride
01 4India
01 4Valid
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : R0-CEP 2020-384 - Rev 00
Status : Valid
Issue Date : 2022-05-17
Type : Chemical
Substance Number : 1029
Certificate Number : CEP 2017-107 - Rev 03
Status : Valid
Issue Date : 2024-04-05
Type : Chemical
Substance Number : 1029
Certificate Number : R1-CEP 2014-057 - Rev 01
Status : Valid
Issue Date : 2021-01-11
Type : Chemical
Substance Number : 1029
Certificate Number : R0-CEP 2021-421 - Rev 00
Status : Valid
Issue Date : 2023-03-10
Type : Chemical
Substance Number : 1029
A (+)-Mexiletine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+)-Mexiletine Hydrochloride, including repackagers and relabelers. The FDA regulates (+)-Mexiletine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+)-Mexiletine 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 (+)-Mexiletine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+)-Mexiletine Hydrochloride supplier is an individual or a company that provides (+)-Mexiletine Hydrochloride active pharmaceutical ingredient (API) or (+)-Mexiletine Hydrochloride finished formulations upon request. The (+)-Mexiletine Hydrochloride suppliers may include (+)-Mexiletine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of (+)-Mexiletine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (+)-Mexiletine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a (+)-Mexiletine Hydrochloride Certificate of Suitability (COS). The purpose of a (+)-Mexiletine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of (+)-Mexiletine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of (+)-Mexiletine Hydrochloride to their clients by showing that a (+)-Mexiletine Hydrochloride CEP has been issued for it. The manufacturer submits a (+)-Mexiletine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a (+)-Mexiletine Hydrochloride CEP holder for the record. Additionally, the data presented in the (+)-Mexiletine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the (+)-Mexiletine Hydrochloride DMF.
A (+)-Mexiletine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. (+)-Mexiletine 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 (+)-Mexiletine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering (+)-Mexiletine Hydrochloride
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