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
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
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PharmaCompass offers a list of Naratriptan Hydrochloride 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 Naratriptan Hydrochloride manufacturer or Naratriptan Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Naratriptan Hydrochloride manufacturer or Naratriptan Hydrochloride supplier.
PharmaCompass also assists you with knowing the Naratriptan Hydrochloride API Price utilized in the formulation of products. Naratriptan Hydrochloride API Price is not always fixed or binding as the Naratriptan Hydrochloride Price is obtained through a variety of data sources. The Naratriptan Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CS-2132 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-2132, including repackagers and relabelers. The FDA regulates CS-2132 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-2132 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 CS-2132 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CS-2132 supplier is an individual or a company that provides CS-2132 active pharmaceutical ingredient (API) or CS-2132 finished formulations upon request. The CS-2132 suppliers may include CS-2132 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-2132 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 CS-2132 Drug Master File in Japan (CS-2132 JDMF) empowers CS-2132 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 CS-2132 JDMF during the approval evaluation for pharmaceutical products. At the time of CS-2132 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 CS-2132 suppliers with JDMF on PharmaCompass.
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