DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1USV Private Limited
01 2Naratriptan Hydrochloride
01 2India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 304MF10063
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2022-04-06
Latest Date of Registration : 2022-04-06
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
Registration Number : 301MF10038
Registrant's Address : Arvind Vithal Gandhi Chowk,B. S. D. Marg, Govandi, Mumbai-400 088, INDIA.
Initial Date of Registration : 2019-07-31
Latest Date of Registration : 2019-07-31
A Naratriptan Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naratriptan Hydrochloride, including repackagers and relabelers. The FDA regulates Naratriptan Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naratriptan Hydrochloride 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 Naratriptan Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naratriptan Hydrochloride supplier is an individual or a company that provides Naratriptan Hydrochloride active pharmaceutical ingredient (API) or Naratriptan Hydrochloride finished formulations upon request. The Naratriptan Hydrochloride suppliers may include Naratriptan Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Naratriptan Hydrochloride 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 Naratriptan Hydrochloride Drug Master File in Japan (Naratriptan Hydrochloride JDMF) empowers Naratriptan Hydrochloride 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 Naratriptan Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Naratriptan Hydrochloride 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 Naratriptan Hydrochloride suppliers with JDMF on PharmaCompass.
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