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Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected. 
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01 Malladi Drugs & Pharmaceuticals Limited (1)
01 Pseudoephedrine (1)
01 India (1)
Iran Expo
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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 MolPort-001-684-474 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-684-474, including repackagers and relabelers. The FDA regulates MolPort-001-684-474 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-684-474 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 MolPort-001-684-474 supplier is an individual or a company that provides MolPort-001-684-474 active pharmaceutical ingredient (API) or MolPort-001-684-474 finished formulations upon request. The MolPort-001-684-474 suppliers may include MolPort-001-684-474 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 MolPort-001-684-474 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MolPort-001-684-474 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 MolPort-001-684-474 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 MolPort-001-684-474 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-001-684-474 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of MolPort-001-684-474 suppliers with NDC on PharmaCompass.
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