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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PharmaCompass offers a list of Imipramine Hydrochloride 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 Imipramine Hydrochloride manufacturer or Imipramine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Imipramine Hydrochloride API Price utilized in the formulation of products. Imipramine Hydrochloride API Price is not always fixed or binding as the Imipramine Hydrochloride Price is obtained through a variety of data sources. The Imipramine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Imidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imidol, including repackagers and relabelers. The FDA regulates Imidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imidol 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 Imidol supplier is an individual or a company that provides Imidol active pharmaceutical ingredient (API) or Imidol finished formulations upon request. The Imidol suppliers may include Imidol API manufacturers, exporters, distributors and traders.
click here to find a list of Imidol 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 Imidol Drug Master File in Japan (Imidol JDMF) empowers Imidol 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 Imidol JDMF during the approval evaluation for pharmaceutical products. At the time of Imidol 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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