Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1Malladi Drugs & Pharmaceuticals Limited
02 1Cheng Fong Chemical Co., Ltd.
03 1Embio Limited
04 1Professional Compounding Centers of America
05 1Professional Compounding Centers of America dba PCCA
06 5Siegfried PharmaChemikalien Minden GmbH
07 1Spectrum Laboratory Products, Inc.
08 1Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.
01 2PSEUDOEPHEDRINE HYDROCHLORIDE
02 9Pseudoephedrine Hydrochloride
03 1Pseudoephedrine hydrochloride
01 2China
02 2India
03 5Switzerland
04 1U.S.A
05 2United Kingdom
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
NDC Package Code : 57218-801
Start Marketing Date : 1995-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58747-7538
Start Marketing Date : 1992-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60646-102
Start Marketing Date : 1998-12-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0125
Start Marketing Date : 2021-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1159
Start Marketing Date : 2013-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 65724-4400
Start Marketing Date : 2010-03-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65724-4401
Start Marketing Date : 2002-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65724-4407
Start Marketing Date : 2011-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65724-4415
Start Marketing Date : 2002-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-6110
Start Marketing Date : 1992-10-01
End Marketing Date : 2025-08-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Pseudoephedrine 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 Pseudoephedrine Hydrochloride manufacturer or Pseudoephedrine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Pseudoephedrine Hydrochloride API Price utilized in the formulation of products. Pseudoephedrine Hydrochloride API Price is not always fixed or binding as the Pseudoephedrine Hydrochloride Price is obtained through a variety of data sources. The Pseudoephedrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pseudoephedrine, (+)- manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pseudoephedrine, (+)-, including repackagers and relabelers. The FDA regulates Pseudoephedrine, (+)- manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pseudoephedrine, (+)- 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, (+)- supplier is an individual or a company that provides Pseudoephedrine, (+)- active pharmaceutical ingredient (API) or Pseudoephedrine, (+)- finished formulations upon request. The Pseudoephedrine, (+)- suppliers may include Pseudoephedrine, (+)- 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, (+)- as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pseudoephedrine, (+)- 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, (+)- 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, (+)- and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pseudoephedrine, (+)- NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pseudoephedrine, (+)- suppliers with NDC on PharmaCompass.
We have 7 companies offering Pseudoephedrine, (+)-
Get in contact with the supplier of your choice:
