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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PharmaCompass offers a list of Pseudoephedrine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pseudoephedrine Hydrochloride manufacturer or Pseudoephedrine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Pseudoephedrine Hydrochloride API Price utilized in the formulation of products. Pseudoephedrine Hydrochloride API Price is not always fixed or binding as the Pseudoephedrine Hydrochloride Price is obtained through a variety of data sources. The Pseudoephedrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MYFED manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MYFED, including repackagers and relabelers. The FDA regulates MYFED manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MYFED 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 MYFED supplier is an individual or a company that provides MYFED active pharmaceutical ingredient (API) or MYFED finished formulations upon request. The MYFED suppliers may include MYFED API manufacturers, exporters, distributors and traders.
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A MYFED written confirmation (MYFED WC) is an official document issued by a regulatory agency to a MYFED manufacturer, verifying that the manufacturing facility of a MYFED active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting MYFED APIs or MYFED finished pharmaceutical products to another nation, regulatory agencies frequently require a MYFED WC (written confirmation) as part of the regulatory process.
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