01 1R L Fine Chem Pvt. Ltd.
01 1Fluphenazine Decanoate
01 1India
Registration Number : 305MF10003
Registrant's Address : RLFC HOUSE, plot no. C-10, 1st Cross, KSSIDC Industrial Estate, Yelahanka New Town, B...
Initial Date of Registration : 2023-01-11
Latest Date of Registration : 2023-01-11
A Fluphenazine Decanoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluphenazine Decanoate, including repackagers and relabelers. The FDA regulates Fluphenazine Decanoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluphenazine Decanoate 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 Fluphenazine Decanoate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluphenazine Decanoate supplier is an individual or a company that provides Fluphenazine Decanoate active pharmaceutical ingredient (API) or Fluphenazine Decanoate finished formulations upon request. The Fluphenazine Decanoate suppliers may include Fluphenazine Decanoate API manufacturers, exporters, distributors and traders.
click here to find a list of Fluphenazine Decanoate 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 Fluphenazine Decanoate Drug Master File in Japan (Fluphenazine Decanoate JDMF) empowers Fluphenazine Decanoate 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 Fluphenazine Decanoate JDMF during the approval evaluation for pharmaceutical products. At the time of Fluphenazine Decanoate 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 Fluphenazine Decanoate suppliers with JDMF on PharmaCompass.
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