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 : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Pseudoephedrine 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 manufacturer or Pseudoephedrine supplier for your needs.
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A Eltor 120 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eltor 120, including repackagers and relabelers. The FDA regulates Eltor 120 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eltor 120 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 Eltor 120 supplier is an individual or a company that provides Eltor 120 active pharmaceutical ingredient (API) or Eltor 120 finished formulations upon request. The Eltor 120 suppliers may include Eltor 120 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 Eltor 120 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Eltor 120 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 Eltor 120 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 Eltor 120 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Eltor 120 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Eltor 120 suppliers with NDC on PharmaCompass.
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