01 2Divi’s Laboratories
02 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
01 1Naproxen (BP/USP/Ph. Eur)
02 1Naproxen (Ph. Eur)
03 1Naproxen IH
01 1WC-0023
02 1WC-0030
03 1WC-0031
01 3India
Date of Issue : 2019-06-26
Valid Till : 2022-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Sy.No.1/22, 2/1 To 5, 6 to 18, 61 to 69, Pydibhimavaram Village, Ranasthalam, Sr...
Date of Issue : 2022-06-16
Valid Till : 2025-06-16
Written Confirmation Number : WC-0031
Address of the Firm : Unit-Lingojigudem (V) Choutuppal (M) Nalgonda District Talangana State India
Date of Issue : 2019-06-17
Valid Till : 2022-06-16
Written Confirmation Number : WC-0030
Address of the Firm : Unit-II, Annavaram(Post), Chippada Village, Beemunipatnam Mandal, Visakhapatan...
63
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.
A Feminax Ultra written confirmation (Feminax Ultra WC) is an official document issued by a regulatory agency to a Feminax Ultra manufacturer, verifying that the manufacturing facility of a Feminax Ultra active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Feminax Ultra APIs or Feminax Ultra finished pharmaceutical products to another nation, regulatory agencies frequently require a Feminax Ultra WC (written confirmation) as part of the regulatory process.
click here to find a list of Feminax Ultra suppliers with Written Confirmation (WC) on PharmaCompass.
We have 2 companies offering Feminax Ultra
Get in contact with the supplier of your choice:
