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 Harika Drugs Private Limited
03 1Keshava Organics
04 1M/s Zentiva Private Limited
01 1Pheniramine Maleate BP
02 1Pheniramine Maleate BP/EP/USP
03 1Pheniramine Maleate BP/EP/USP/JP
04 1Pheniramine Maleate Ph. Eur
01 1WC-0133
02 1WC-0179n
03 1WC-0218n
04 1WC-0244
01 4India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Pheniramine Maleate BP/EP/USP/JP
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, ...
Harika Drugs has been providing a qualitative range of Bulk Drugs/ APIs since 1993.
Date of Issue : 2022-07-27
Valid Till : 2025-07-29
Written Confirmation Number : WC-0179n
Address of the Firm : Sy. No. 165/A & 165/E, Gummadidala Village, Sangareddy District, Telangana State...
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 : 2023-03-11
Valid Till : 2026-10-14
Written Confirmation Number : WC-0133
Address of the Firm : Plot No 3501 to 3515, 6301 to 6313 & 16 Meter Road/C, G.I.D.C Estate, Ankleshwar...
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PharmaCompass offers a list of Pheniramine 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 Pheniramine Maleate manufacturer or Pheniramine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Pheniramine Maleate API Price utilized in the formulation of products. Pheniramine Maleate API Price is not always fixed or binding as the Pheniramine Maleate Price is obtained through a variety of data sources. The Pheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trimetose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimetose, including repackagers and relabelers. The FDA regulates Trimetose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimetose 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 Trimetose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimetose supplier is an individual or a company that provides Trimetose active pharmaceutical ingredient (API) or Trimetose finished formulations upon request. The Trimetose suppliers may include Trimetose API manufacturers, exporters, distributors and traders.
click here to find a list of Trimetose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trimetose written confirmation (Trimetose WC) is an official document issued by a regulatory agency to a Trimetose manufacturer, verifying that the manufacturing facility of a Trimetose active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Trimetose APIs or Trimetose finished pharmaceutical products to another nation, regulatory agencies frequently require a Trimetose WC (written confirmation) as part of the regulatory process.
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