Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.

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01 1Malladi Drugs & Pharmaceuticals Limited
02 2M/s Supriya Lifescience Ltd
03 1Keshava Organics
04 1M/s Auro Laboratories Limited
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01 1Chlorphenamine Maleate BP/IP
02 1Chlorphenamine Maleate EP
03 1Chlorpheniramine Maleate BP/EP/USP
04 1Chlorpheniramine Maleate BP/Ph. Eur
05 1Chlorpheniramine Maleate USP
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01 1WC-0085
02 2WC-0218
03 1WC-0244
04 1WC-0318
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01 5India
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Date of Issue : 2026-04-10
Valid Till : 2029-04-09
Written Confirmation Number : WC-0318
Address of the Firm : Unit 5, Plot No. 49, 50, 55 & 56, IDA, Gajulamandyam, Attur (PO) Renigunta-51752...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Chlorpheniramine Maleate BP/Ph. Eur
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, ...
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, ...
Date of Issue : 2026-01-13
Valid Till : 2028-08-04
Written Confirmation Number : WC-0085
Address of the Firm : K-56 M.I.D.C. Boisar, Tarapur, Thane -401506,Taluka: MIDC Tarapur Boisar,Distric...

Chlorpheniramine Maleate BP/EP/USP
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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A CHLORPHENIRAMINE BASE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CHLORPHENIRAMINE BASE, including repackagers and relabelers. The FDA regulates CHLORPHENIRAMINE BASE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CHLORPHENIRAMINE BASE 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 BASE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CHLORPHENIRAMINE BASE supplier is an individual or a company that provides CHLORPHENIRAMINE BASE active pharmaceutical ingredient (API) or CHLORPHENIRAMINE BASE finished formulations upon request. The CHLORPHENIRAMINE BASE suppliers may include CHLORPHENIRAMINE BASE API manufacturers, exporters, distributors and traders.
click here to find a list of CHLORPHENIRAMINE BASE suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A CHLORPHENIRAMINE BASE written confirmation (CHLORPHENIRAMINE BASE WC) is an official document issued by a regulatory agency to a CHLORPHENIRAMINE BASE manufacturer, verifying that the manufacturing facility of a CHLORPHENIRAMINE BASE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CHLORPHENIRAMINE BASE APIs or CHLORPHENIRAMINE BASE finished pharmaceutical products to another nation, regulatory agencies frequently require a CHLORPHENIRAMINE BASE WC (written confirmation) as part of the regulatory process.
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