Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1M/s.RA Chem Pharma Ltd
02 1M/s. Punjab Chemicals and Crop Protection Ltd.,
01 1Drotaverine Hydrochloride (IH)
02 1Drotaverine Hydrochloride IH
01 1WC-0051
02 1WC-0150
01 2India
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 : R. S. No. 50/1, Mukteswarapuram (V), Jaggalahpet (M), Krishna -District- 521175,...
Drotaverine Hydrochloride (IH)
Date of Issue : 2017-04-11
Valid Till : 2020-04-10
Written Confirmation Number : WC-0051
Address of the Firm : Village- Kolimajra, & Samalheri, P.O. - Lalru, Tehsil- Derabassi, Distt.- Mohali...
A Drotaverine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Drotaverine, including repackagers and relabelers. The FDA regulates Drotaverine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Drotaverine 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 Drotaverine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Drotaverine supplier is an individual or a company that provides Drotaverine active pharmaceutical ingredient (API) or Drotaverine finished formulations upon request. The Drotaverine suppliers may include Drotaverine API manufacturers, exporters, distributors and traders.
click here to find a list of Drotaverine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Drotaverine written confirmation (Drotaverine WC) is an official document issued by a regulatory agency to a Drotaverine manufacturer, verifying that the manufacturing facility of a Drotaverine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Drotaverine APIs or Drotaverine finished pharmaceutical products to another nation, regulatory agencies frequently require a Drotaverine WC (written confirmation) as part of the regulatory process.
click here to find a list of Drotaverine suppliers with Written Confirmation (WC) on PharmaCompass.
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