01 2Divi’s Laboratories
02 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
03 1M/s. Mylan Laboratories Ltd.,
01 1Naproxen Sodium (Ph. Eur)
02 1Naproxen Sodium (Ph. Eur) 0
03 1Naproxen Sodium (Ph. Eur/USP)
04 1Naproxen Sodium (Ph. Eur/USP/BP)
01 1WC-0015
02 1WC-0023
03 1WC-0030
04 1WC-0031
01 4India
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
Naproxen Sodium (Ph. Eur/USP/BP)
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...
Date of Issue : 2019-06-03
Valid Till : 2022-06-02
Written Confirmation Number : WC-0015
Address of the Firm : Unit VIII, G Chodevaram (V), Pusapatirega (Mandal), Vizianagaram Dist.,-535204, ...
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PharmaCompass offers a list of Naproxen Sodium 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 Sodium manufacturer or Naproxen Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Naproxen Sodium API Price utilized in the formulation of products. Naproxen Sodium API Price is not always fixed or binding as the Naproxen Sodium Price is obtained through a variety of data sources. The Naproxen Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MNPA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MNPA, including repackagers and relabelers. The FDA regulates MNPA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MNPA 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 MNPA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MNPA supplier is an individual or a company that provides MNPA active pharmaceutical ingredient (API) or MNPA finished formulations upon request. The MNPA suppliers may include MNPA API manufacturers, exporters, distributors and traders.
click here to find a list of MNPA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MNPA written confirmation (MNPA WC) is an official document issued by a regulatory agency to a MNPA manufacturer, verifying that the manufacturing facility of a MNPA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting MNPA APIs or MNPA finished pharmaceutical products to another nation, regulatory agencies frequently require a MNPA WC (written confirmation) as part of the regulatory process.
click here to find a list of MNPA suppliers with Written Confirmation (WC) on PharmaCompass.
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