Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1M/s. Malladi Drugs & Pharmaceuticals Limited
02 1M/s. Aarti Pharmalabs Limited
03 1Divi’s Laboratories
04 1M/s Vital Laboratories Pvt ltd
05 1M/s. Unichem Lab. Ltd.
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Phenylephrine Hydrochloride (USP,BP,EP, 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, SICOT Industrial Complex, Ranipet 632 403, Ranipet District, Ta...
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Phenylephrine Hydrochloride EP/BP/IP/USP
Date of Issue : 2023-01-06
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm : Plot No. E-50, 50/1 and 59/1, Unit — IV, MIDC, Tarapur — 401506, Taluka: Pal...
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PharmaCompass offers a list of Phenylephrine 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 Phenylephrine Hydrochloride manufacturer or Phenylephrine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenylephrine Hydrochloride manufacturer or Phenylephrine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Phenylephrine Hydrochloride API Price utilized in the formulation of products. Phenylephrine Hydrochloride API Price is not always fixed or binding as the Phenylephrine Hydrochloride Price is obtained through a variety of data sources. The Phenylephrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sudafed PE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sudafed PE, including repackagers and relabelers. The FDA regulates Sudafed PE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sudafed PE 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 Sudafed PE supplier is an individual or a company that provides Sudafed PE active pharmaceutical ingredient (API) or Sudafed PE finished formulations upon request. The Sudafed PE suppliers may include Sudafed PE API manufacturers, exporters, distributors and traders.
click here to find a list of Sudafed PE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sudafed PE written confirmation (Sudafed PE WC) is an official document issued by a regulatory agency to a Sudafed PE manufacturer, verifying that the manufacturing facility of a Sudafed PE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sudafed PE APIs or Sudafed PE finished pharmaceutical products to another nation, regulatory agencies frequently require a Sudafed PE WC (written confirmation) as part of the regulatory process.
click here to find a list of Sudafed PE suppliers with Written Confirmation (WC) on PharmaCompass.
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