01 2R L FINE CHEM Pvt. Ltd.
01 1Imipramine Hydrochloride
02 1Imipramine hydrochloride
01 2India
Registration Number : 304MF10070
Registrant's Address : RLFC HOUSE, plot no. C-10, 1st Cross, KSSIDC Industrial Estate, Yelahanka New Town, B...
Initial Date of Registration : 2022-05-06
Latest Date of Registration : 2022-05-06
Registration Number : 222MF10074
Registrant's Address : RLFC HOUSE, plot no. C-10, 1st Cross, KSSIDC Industrial Estate, Yelahanka New Town, B...
Initial Date of Registration : 2010-03-02
Latest Date of Registration : 2010-03-02
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A imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil, including repackagers and relabelers. The FDA regulates imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil supplier is an individual or a company that provides imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil active pharmaceutical ingredient (API) or imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil finished formulations upon request. The imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil suppliers may include imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil API manufacturers, exporters, distributors and traders.
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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 imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil Drug Master File in Japan (imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil JDMF) empowers imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil 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 imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil JDMF during the approval evaluation for pharmaceutical products. At the time of imipramine hydrochloride,berkomine,deprinol,dyna-zina,imiprin,iramil JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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