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 Feminax Ultra manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Feminax Ultra, including repackagers and relabelers. The FDA regulates Feminax Ultra manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Feminax Ultra 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 Feminax Ultra manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Feminax Ultra supplier is an individual or a company that provides Feminax Ultra active pharmaceutical ingredient (API) or Feminax Ultra finished formulations upon request. The Feminax Ultra suppliers may include Feminax Ultra API manufacturers, exporters, distributors and traders.
click here to find a list of Feminax Ultra 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 Feminax Ultra Drug Master File in Japan (Feminax Ultra JDMF) empowers Feminax Ultra 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 Feminax Ultra JDMF during the approval evaluation for pharmaceutical products. At the time of Feminax Ultra 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 Feminax Ultra suppliers with JDMF on PharmaCompass.
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