01 1R L FINE CHEM Pvt. Ltd.
02 1R L Fine Chem Pvt. Ltd.
01 1Clomipramine Hydrochloride
02 1Clomipramine hydrochloride
01 2India
Registration Number : 218MF10855
Registrant's Address : RLFC HOUSE, plot no. C-10, 1st Cross, KSSIDC Industrial Estate, Yelahanka New Town, B...
Initial Date of Registration : 2006-11-06
Latest Date of Registration : 2007-06-04
Registration Number : 305MF10043
Registrant's Address : RLFC HOUSE, plot no. C-10, 1st Cross, KSSIDC Industrial Estate, Yelahanka New Town, B...
Initial Date of Registration : 2023-04-05
Latest Date of Registration : 2023-04-05
A Clomipramine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clomipramine Hydrochloride, including repackagers and relabelers. The FDA regulates Clomipramine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clomipramine 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 Clomipramine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clomipramine Hydrochloride supplier is an individual or a company that provides Clomipramine Hydrochloride active pharmaceutical ingredient (API) or Clomipramine Hydrochloride finished formulations upon request. The Clomipramine Hydrochloride suppliers may include Clomipramine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Clomipramine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Clomipramine Hydrochloride Drug Master File in Japan (Clomipramine Hydrochloride JDMF) empowers Clomipramine Hydrochloride API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Clomipramine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Clomipramine Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Clomipramine Hydrochloride suppliers with JDMF on PharmaCompass.
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