DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited office and manufacturing site in Mexico
01 1Naproxen
01 1India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 219MF10208
Registrant's Address : Km. 4.5 Carretera Federal Cuernavaca-Cuautla 62578 Jiutepec, Morelos, Mexico
Initial Date of Registration : 2007-06-25
Latest Date of Registration : 2007-06-25
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PharmaCompass offers a list of Naproxen 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 Naproxen manufacturer or Naproxen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Naproxen manufacturer or Naproxen supplier.
PharmaCompass also assists you with knowing the Naproxen API Price utilized in the formulation of products. Naproxen API Price is not always fixed or binding as the Naproxen Price is obtained through a variety of data sources. The Naproxen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tundra manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tundra, including repackagers and relabelers. The FDA regulates Tundra manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tundra 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 Tundra manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tundra supplier is an individual or a company that provides Tundra active pharmaceutical ingredient (API) or Tundra finished formulations upon request. The Tundra suppliers may include Tundra API manufacturers, exporters, distributors and traders.
click here to find a list of Tundra 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 Tundra Drug Master File in Japan (Tundra JDMF) empowers Tundra 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 Tundra JDMF during the approval evaluation for pharmaceutical products. At the time of Tundra 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 Tundra suppliers with JDMF on PharmaCompass.
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