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. Harika Drugs Private Limited
03 1M/s. Keshav Organics Pvt.Ltd
04 1M/s. R. L. Fine Chem Pvt Ltd
05 1M/s. Auro Laboratories Ltd
01 1Carbinoxamide maleate USP
02 1Chlorpheniramine Maleate (BP, EP, USP)
03 1Chlorpheniramine Maleate (Ph. Eur.)
04 1Chlorpheniramine Maleate BP/USP/EP
05 1Dexbrompheniramine Maieate (USP)
01 1WC-0085
02 1WC-0139
03 1WC-0179
04 1WC-0218
05 1WC-244
01 5India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Chlorpheniramine 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, ...
Harika Drugs has been providing a qualitative range of Bulk Drugs/ APIs since 1993.
Chlorpheniramine Maleate (Ph. Eur.)
Date of Issue : 2022-07-27
Valid Till : 2025-07-29
Written Confirmation Number : WC-0179
Address of the Firm : Sy.No.165/A & 165/E, Gummadidala Village, Medak Dist,Talangana State, India
Chlorpheniramine Maleate BP/USP/EP
Date of Issue : 2022-08-08
Valid Till : 2025-08-04
Written Confirmation Number : WC-0085
Address of the Firm : K-56, MIDC, Tarapur, Dist. - Thane-401 506
Dexbrompheniramine Maieate (USP)
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
Date of Issue : 2019-07-22
Valid Till : 2022-07-22
Written Confirmation Number : WC-0139
Address of the Firm : # 15, KHB Industrial Area, Yelahanka, Bangalore-560 064
A Chlorpheniramine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorpheniramine Maleate, including repackagers and relabelers. The FDA regulates Chlorpheniramine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorpheniramine Maleate 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 Maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorpheniramine Maleate supplier is an individual or a company that provides Chlorpheniramine Maleate active pharmaceutical ingredient (API) or Chlorpheniramine Maleate finished formulations upon request. The Chlorpheniramine Maleate suppliers may include Chlorpheniramine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorpheniramine Maleate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chlorpheniramine Maleate written confirmation (Chlorpheniramine Maleate WC) is an official document issued by a regulatory agency to a Chlorpheniramine Maleate manufacturer, verifying that the manufacturing facility of a Chlorpheniramine Maleate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Chlorpheniramine Maleate APIs or Chlorpheniramine Maleate finished pharmaceutical products to another nation, regulatory agencies frequently require a Chlorpheniramine Maleate WC (written confirmation) as part of the regulatory process.
click here to find a list of Chlorpheniramine Maleate suppliers with Written Confirmation (WC) on PharmaCompass.
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