Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1Malladi Drugs & Pharmaceuticals Limited
01 1Pseudoephedrine
01 1India
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
NDC Package Code : 57218-500
Start Marketing Date : 2003-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Pseudoephedrine polistirex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pseudoephedrine polistirex, including repackagers and relabelers. The FDA regulates Pseudoephedrine polistirex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pseudoephedrine polistirex 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 Pseudoephedrine polistirex supplier is an individual or a company that provides Pseudoephedrine polistirex active pharmaceutical ingredient (API) or Pseudoephedrine polistirex finished formulations upon request. The Pseudoephedrine polistirex suppliers may include Pseudoephedrine polistirex API manufacturers, exporters, distributors and traders.
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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 Pseudoephedrine polistirex as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pseudoephedrine polistirex 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 Pseudoephedrine polistirex 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 Pseudoephedrine polistirex and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pseudoephedrine polistirex NDC to their finished compounded human drug products, they may choose to do so.
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