Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1M/s Supriya Lifescience Ltd
02 1M/s Vital Laboratories Pvt ltd
03 1M/s RPG Life Sciences Ltd
01 1Nicorandil BP/Ph. Eur
02 1Nicorandil IH/BP/EP/JP
03 1Nicorandil JP
01 1WC-0056
02 1WC-0218
03 1WC-0300
01 3India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Date of Issue : 2025-09-02
Valid Till : 2028-07-02
Written Confirmation Number : WC-0218
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
Vital Laboratories – Trusted Global Manufacturer of Quinine and Antimalarial APIs Since 1998
Date of Issue : 2024-05-20
Valid Till : 2027-01-08
Written Confirmation Number : WC-0300
Address of the Firm : Plot No. 1710, Phase-lll, G.I.D.C Estate, Vapi-396195, Dist.-Valsad, Gujarat, In...
Date of Issue : 2025-11-06
Valid Till : 2028-07-28
Written Confirmation Number : WC-0056
Address of the Firm : 25 MIDC Land, Thane Belapur Road, Navi Mumbai - 400703, Taluka: Pawvane, Distric...
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PharmaCompass offers a list of Nicorandil 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 Nicorandil manufacturer or Nicorandil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nicorandil manufacturer or Nicorandil supplier.
PharmaCompass also assists you with knowing the Nicorandil API Price utilized in the formulation of products. Nicorandil API Price is not always fixed or binding as the Nicorandil Price is obtained through a variety of data sources. The Nicorandil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N0837 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0837, including repackagers and relabelers. The FDA regulates N0837 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0837 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 N0837 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N0837 supplier is an individual or a company that provides N0837 active pharmaceutical ingredient (API) or N0837 finished formulations upon request. The N0837 suppliers may include N0837 API manufacturers, exporters, distributors and traders.
click here to find a list of N0837 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A N0837 written confirmation (N0837 WC) is an official document issued by a regulatory agency to a N0837 manufacturer, verifying that the manufacturing facility of a N0837 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting N0837 APIs or N0837 finished pharmaceutical products to another nation, regulatory agencies frequently require a N0837 WC (written confirmation) as part of the regulatory process.
click here to find a list of N0837 suppliers with Written Confirmation (WC) on PharmaCompass.
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