With Virupaksha, you get a quality product with on-time delivery.
01 1VIRUPAKSHA ORGANICS LIMITED
02 1EUROAPI Germany GmbH
03 1Granules India Ltd
04 1Aurobindo Pharma Limited
05 1Chemeca Drugs Private Limited
06 1Cipla Ltd.
07 5Dipharma Francis Srl
08 1Hetero Drugs Limited
09 1Jubilant Pharmova Limited
10 1Morepen Laboratories Limited
11 1Mylan Laboratories Limited
12 2Professional Compounding Centers of America dba PCCA
13 1Synthimed Labs Private Limited
14 1Tianish Laboratories Private Limited
15 1Vasudha Pharma Chem Limited
01 3FEXOFENADINE HYDROCHLORIDE
02 15Fexofenadine Hydrochloride
03 2fexofenadine hydrochloride
01 1France
02 11India
03 5Italy
04 1U.S.A
05 2United Kingdom
With Virupaksha, you get a quality product with on-time delivery.
NDC Package Code : 51686-0001
Start Marketing Date : 2007-10-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82348-104
Start Marketing Date : 1997-12-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-002
Start Marketing Date : 2018-06-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0107
Start Marketing Date : 2006-12-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0637
Start Marketing Date : 2016-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0638
Start Marketing Date : 2016-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0651
Start Marketing Date : 2018-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-1111
Start Marketing Date : 2014-05-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0016
Start Marketing Date : 2016-08-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0044
Start Marketing Date : 2020-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Fexofenadine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fexofenadine Hydrochloride, including repackagers and relabelers. The FDA regulates Fexofenadine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fexofenadine Hydrochloride 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 Fexofenadine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fexofenadine Hydrochloride supplier is an individual or a company that provides Fexofenadine Hydrochloride active pharmaceutical ingredient (API) or Fexofenadine Hydrochloride finished formulations upon request. The Fexofenadine Hydrochloride suppliers may include Fexofenadine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Fexofenadine Hydrochloride 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 Fexofenadine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fexofenadine Hydrochloride 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 Fexofenadine Hydrochloride 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 Fexofenadine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fexofenadine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fexofenadine Hydrochloride suppliers with NDC on PharmaCompass.
We have 15 companies offering Fexofenadine Hydrochloride
Get in contact with the supplier of your choice:
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