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