01 1M/s. Keshav Organics Pvt.Ltd
01 1Chlorpheniramine Maieate (USP/BP/Ph.Eur)
01 1WC-244
01 1India
Chlorpheniramine 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
A AC1L1QK4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AC1L1QK4, including repackagers and relabelers. The FDA regulates AC1L1QK4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AC1L1QK4 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A AC1L1QK4 supplier is an individual or a company that provides AC1L1QK4 active pharmaceutical ingredient (API) or AC1L1QK4 finished formulations upon request. The AC1L1QK4 suppliers may include AC1L1QK4 API manufacturers, exporters, distributors and traders.
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A AC1L1QK4 written confirmation (AC1L1QK4 WC) is an official document issued by a regulatory agency to a AC1L1QK4 manufacturer, verifying that the manufacturing facility of a AC1L1QK4 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AC1L1QK4 APIs or AC1L1QK4 finished pharmaceutical products to another nation, regulatory agencies frequently require a AC1L1QK4 WC (written confirmation) as part of the regulatory process.
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