Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
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01 1M/s Biophore India Pharmaceuticals Pvt ltd
02 1M/s Biophore Indian Pharmaceutical Pvt Ltd
03 1M/s Cohance Lifesciences Limited
04 1M/s Alembic Pharmaceuticals Limited
05 1M/s Hetero Drugs Limited
06 1M/sAlembic Pharmaceuticals limited
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01 1Mexiletine Hydrochloride EP
02 1Mexiletine Hydrochloride IH
03 1Mexiletine Hydrochloride Ph. Eur
04 1Mexiletine Hydrochloride USP
05 1Mexiletine Hydrochloride USP/Ph.Eur
06 1Mexiletine IH
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01 1WC-0066
02 1WC-0081
03 1WC-0082
04 1WC-0150
05 1WC-0511
06 1WC-511n
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01 6India
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Date of Issue : 2025-02-27
Valid Till : 2028-02-26
Written Confirmation Number : WC-0511
Address of the Firm : Plot No. 80A, Road No.5, Jawaharlal Nehru Pharma City, E. Bonangi (V), Parawada ...
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Date of Issue : 2022-07-07
Valid Till : 2025-07-21
Written Confirmation Number : WC-0150
Address of the Firm : APIUnit-l,R.SNo50/1,Mukteswarapuram Village, Jaggaiahpet Mandal, NTRDistrict-521...
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Date of Issue : 2025-02-27
Valid Till : 2028-02-26
Written Confirmation Number : WC-511n
Address of the Firm : Plot No. 80A, Road No.5, Jawaharlal Nehru Pharma City, E. Bonangi (V), Parawada ...
Date of Issue : 2022-07-26
Valid Till : 2025-07-02
Written Confirmation Number : WC-0081
Address of the Firm : API Division Panelav, Tal-Halol, Dist-Panchmahal, Gujarat, India
Mexiletine Hydrochloride Ph. Eur
Date of Issue : 2022-06-17
Valid Till : 2025-02-07
Written Confirmation Number : WC-0082
Address of the Firm : Karakhadi Plot No. 842-843, At - Karakhdi, Tal. - Padra, Dist - Vadodara 391 450...
Mexiletine Hydrochloride USP/Ph.Eur
Date of Issue : 2022-09-30
Valid Till : 2025-08-08
Written Confirmation Number : WC-0066
Address of the Firm : Plot No 1, Hetero Infrastructure SEZ Ltd., N. Narasapuram, Anakapalli -531081, A...
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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 written confirmation (Ritalmex WC) is an official document issued by a regulatory agency to a Ritalmex manufacturer, verifying that the manufacturing facility of a Ritalmex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ritalmex APIs or Ritalmex finished pharmaceutical products to another nation, regulatory agencies frequently require a Ritalmex WC (written confirmation) as part of the regulatory process.
click here to find a list of Ritalmex suppliers with Written Confirmation (WC) on PharmaCompass.
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