01 1R L FINE CHEM Pvt. Ltd.
01 1Full phenazine decanoate ester "RL"
01 1India
Registration Number : 229MF10096
Registrant's Address : RLFC HOUSE, plot no. C-10, 1st Cross, KSSIDC Industrial Estate, Yelahanka New Town, B...
Initial Date of Registration : 2017-05-16
Latest Date of Registration : 2020-02-13
A Perphenazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Perphenazine, including repackagers and relabelers. The FDA regulates Perphenazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Perphenazine 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 Perphenazine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Perphenazine supplier is an individual or a company that provides Perphenazine active pharmaceutical ingredient (API) or Perphenazine finished formulations upon request. The Perphenazine suppliers may include Perphenazine API manufacturers, exporters, distributors and traders.
click here to find a list of Perphenazine 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 Perphenazine Drug Master File in Japan (Perphenazine JDMF) empowers Perphenazine 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 Perphenazine JDMF during the approval evaluation for pharmaceutical products. At the time of Perphenazine 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 Perphenazine suppliers with JDMF on PharmaCompass.
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