Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1M/s Malladi Drugs and Pharmaceuticals Limited
02 1M/s Embio Limited
01 1Pseudoephedrine Hydrochloride IP/SP/Ph. Eur/USP/JPC
02 1Pseudoephedrine Hydrochloride USP/BP/Ph. Eur/IP
01 1WC-0046
02 1WC-0093
01 2India
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Pseudoephedrine Hydrochloride USP/BP/Ph. Eur/IP
Date of Issue : 2022-06-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0093
Address of the Firm : Unit -3, 7B & 7C, SIPCOT Industrial Complex, Ranipet -632403, Ranipet District, ...
Pseudoephedrine Hydrochloride IP/SP/Ph. Eur/USP/JPC
Date of Issue : 2022-01-09
Valid Till : 2025-07-28
Written Confirmation Number : WC-0046
Address of the Firm : E-21, MIDC, Indt. Estate, Mahad-402 309, Taluka: Mahad, District: Raigad, Mahara...
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A TRIPROLIDINE; PSEUDOEPHEDRINE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TRIPROLIDINE; PSEUDOEPHEDRINE, including repackagers and relabelers. The FDA regulates TRIPROLIDINE; PSEUDOEPHEDRINE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TRIPROLIDINE; PSEUDOEPHEDRINE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A TRIPROLIDINE; PSEUDOEPHEDRINE supplier is an individual or a company that provides TRIPROLIDINE; PSEUDOEPHEDRINE active pharmaceutical ingredient (API) or TRIPROLIDINE; PSEUDOEPHEDRINE finished formulations upon request. The TRIPROLIDINE; PSEUDOEPHEDRINE suppliers may include TRIPROLIDINE; PSEUDOEPHEDRINE API manufacturers, exporters, distributors and traders.
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A TRIPROLIDINE; PSEUDOEPHEDRINE written confirmation (TRIPROLIDINE; PSEUDOEPHEDRINE WC) is an official document issued by a regulatory agency to a TRIPROLIDINE; PSEUDOEPHEDRINE manufacturer, verifying that the manufacturing facility of a TRIPROLIDINE; PSEUDOEPHEDRINE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting TRIPROLIDINE; PSEUDOEPHEDRINE APIs or TRIPROLIDINE; PSEUDOEPHEDRINE finished pharmaceutical products to another nation, regulatory agencies frequently require a TRIPROLIDINE; PSEUDOEPHEDRINE WC (written confirmation) as part of the regulatory process.
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