Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
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01 2M/s Supriya Lifescience Ltd
02 2Keshava Organics
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01 1Mepyramine Maleate BP/EP
02 1Pyrilamine Maleate BP/EP
03 2Pyrilamine Maleate USP
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01 2WC-0218n
02 2WC-0244
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01 4India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218n
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218n
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
Date of Issue : 2022-12-09
Valid Till : 2025-07-02
Written Confirmation Number : WC-0244
Address of the Firm : Plot No. T-97 & 100, MIDC, Tarapur, -401 506, Taluka: Palghar, Dist-Thane Zone-4
Date of Issue : 2022-12-09
Valid Till : 2025-07-02
Written Confirmation Number : WC-0244
Address of the Firm : Plot No. T-97 & 100, MIDC, Tarapur, -401 506, Taluka: Palghar, Dist-Thane Zone-4
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PharmaCompass offers a list of Pyrilamine Maleate 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 Pyrilamine Maleate manufacturer or Pyrilamine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Pyrilamine Maleate API Price utilized in the formulation of products. Pyrilamine Maleate API Price is not always fixed or binding as the Pyrilamine Maleate Price is obtained through a variety of data sources. The Pyrilamine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anthisan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anthisan, including repackagers and relabelers. The FDA regulates Anthisan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anthisan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Anthisan supplier is an individual or a company that provides Anthisan active pharmaceutical ingredient (API) or Anthisan finished formulations upon request. The Anthisan suppliers may include Anthisan API manufacturers, exporters, distributors and traders.
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A Anthisan written confirmation (Anthisan WC) is an official document issued by a regulatory agency to a Anthisan manufacturer, verifying that the manufacturing facility of a Anthisan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Anthisan APIs or Anthisan finished pharmaceutical products to another nation, regulatory agencies frequently require a Anthisan WC (written confirmation) as part of the regulatory process.
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