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
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PharmaCompass offers a list of Mexiletine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Mexiletine manufacturer or Mexiletine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mexiletine manufacturer or Mexiletine supplier.
PharmaCompass also assists you with knowing the Mexiletine API Price utilized in the formulation of products. Mexiletine API Price is not always fixed or binding as the Mexiletine Price is obtained through a variety of data sources. The Mexiletine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ritalmex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritalmex, including repackagers and relabelers. The FDA regulates Ritalmex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritalmex 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 Ritalmex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ritalmex supplier is an individual or a company that provides Ritalmex active pharmaceutical ingredient (API) or Ritalmex finished formulations upon request. The Ritalmex suppliers may include Ritalmex API manufacturers, exporters, distributors and traders.
click here to find a list of Ritalmex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ritalmex CEP of the European Pharmacopoeia monograph is often referred to as a Ritalmex Certificate of Suitability (COS). The purpose of a Ritalmex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ritalmex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ritalmex to their clients by showing that a Ritalmex CEP has been issued for it. The manufacturer submits a Ritalmex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ritalmex CEP holder for the record. Additionally, the data presented in the Ritalmex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ritalmex DMF.
A Ritalmex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ritalmex 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 Ritalmex suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering Ritalmex
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