Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1M/s Supriya Lifesience Ltd
02 1M/s. Halcyon Labs Pvt.Ltd.
03 1M/s. Keshav Organics Pvt.Ltd
01 1Dexchlorpheniramine Maieate (USP/BP/Ph.Eur)
02 1Dexchlorpheniramine Maleate (BP/EP/USP)
03 1Dexchlorpheniramine Maleate (USP)
01 1WC-0218
02 1WC-241
03 1WC-244
01 3India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Dexchlorpheniramine Maleate (BP/EP/USP)
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
Dexchlorpheniramine Maleate (USP)
Date of Issue : 2020-02-24
Valid Till : 2022-07-02
Written Confirmation Number : WC-241
Address of the Firm : Plot No. 409, Phase-IV, GIDC Industrial Estate, Naroda, Ahemdabad-382330, Gujara...
Dexchlorpheniramine Maieate (USP/BP/Ph.Eur)
Date of Issue : 2022-12-09
Valid Till : 2025-07-02
Written Confirmation Number : WC-244
Address of the Firm : Plot No. T-97 &T-100, MIDC Tarapur, Dist Thane-401506, Maharshtra
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PharmaCompass also assists you with knowing the Dexchloropheniramine Maleate API Price utilized in the formulation of products. Dexchloropheniramine Maleate API Price is not always fixed or binding as the Dexchloropheniramine Maleate Price is obtained through a variety of data sources. The Dexchloropheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CHLORPHENIRAMINE POLISTIREX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CHLORPHENIRAMINE POLISTIREX, including repackagers and relabelers. The FDA regulates CHLORPHENIRAMINE POLISTIREX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CHLORPHENIRAMINE POLISTIREX 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 CHLORPHENIRAMINE POLISTIREX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CHLORPHENIRAMINE POLISTIREX supplier is an individual or a company that provides CHLORPHENIRAMINE POLISTIREX active pharmaceutical ingredient (API) or CHLORPHENIRAMINE POLISTIREX finished formulations upon request. The CHLORPHENIRAMINE POLISTIREX suppliers may include CHLORPHENIRAMINE POLISTIREX API manufacturers, exporters, distributors and traders.
click here to find a list of CHLORPHENIRAMINE POLISTIREX suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CHLORPHENIRAMINE POLISTIREX written confirmation (CHLORPHENIRAMINE POLISTIREX WC) is an official document issued by a regulatory agency to a CHLORPHENIRAMINE POLISTIREX manufacturer, verifying that the manufacturing facility of a CHLORPHENIRAMINE POLISTIREX active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CHLORPHENIRAMINE POLISTIREX APIs or CHLORPHENIRAMINE POLISTIREX finished pharmaceutical products to another nation, regulatory agencies frequently require a CHLORPHENIRAMINE POLISTIREX WC (written confirmation) as part of the regulatory process.
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