Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak, a,s
02 1Aurobindo Pharma Limited
03 1Glenmark Life Sciences Limited
04 1Hetero Drugs Limited
05 1MSN Laboratories Private Limited
06 1Unichem Laboratories Limited, India
01 6Alfuzosin Hydrochloride
01 1Czech Republic
02 5India
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
NDC Package Code : 63278-0500
Start Marketing Date : 2004-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-206
Start Marketing Date : 2023-12-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-826
Start Marketing Date : 2006-08-10
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0023
Start Marketing Date : 2003-12-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0003
Start Marketing Date : 2010-03-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-019
Start Marketing Date : 2009-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Alfuzosin HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alfuzosin HCl, including repackagers and relabelers. The FDA regulates Alfuzosin HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alfuzosin HCl 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 Alfuzosin HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alfuzosin HCl supplier is an individual or a company that provides Alfuzosin HCl active pharmaceutical ingredient (API) or Alfuzosin HCl finished formulations upon request. The Alfuzosin HCl suppliers may include Alfuzosin HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Alfuzosin HCl 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 Alfuzosin HCl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Alfuzosin HCl 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 Alfuzosin HCl 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 Alfuzosin HCl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Alfuzosin HCl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Alfuzosin HCl suppliers with NDC on PharmaCompass.
We have 6 companies offering Alfuzosin HCl
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