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