Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1Malladi Drugs & Pharmaceuticals Limited
02 1Shenzhen Oriental Pharmaceutical Co., Ltd.
01 1Phenylephrine Bitartrate
02 1Phenylephrine bitartrate
01 1China
02 1India
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
NDC Package Code : 57218-820
Start Marketing Date : 2012-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64431-0004
Start Marketing Date : 2016-10-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Phenylephrine Bitartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phenylephrine Bitartrate, including repackagers and relabelers. The FDA regulates Phenylephrine Bitartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phenylephrine Bitartrate 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 Phenylephrine Bitartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Phenylephrine Bitartrate supplier is an individual or a company that provides Phenylephrine Bitartrate active pharmaceutical ingredient (API) or Phenylephrine Bitartrate finished formulations upon request. The Phenylephrine Bitartrate suppliers may include Phenylephrine Bitartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Phenylephrine Bitartrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Phenylephrine Bitartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Phenylephrine Bitartrate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Phenylephrine Bitartrate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Phenylephrine Bitartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Phenylephrine Bitartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Phenylephrine Bitartrate suppliers with NDC on PharmaCompass.
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