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fexofenadine hydrochloride - 55312-571-39 - (fexofenadine hydrochloride)

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Drug Information of fexofenadine hydrochloride

Product NDC: 55312-571
Proprietary Name: fexofenadine hydrochloride
Non Proprietary Name: fexofenadine hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   fexofenadine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of fexofenadine hydrochloride

Product NDC: 55312-571
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20110414

Package Information of fexofenadine hydrochloride

Package NDC: 55312-571-39
Package Description: 1 BOTTLE in 1 CARTON (55312-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE

NDC Information of fexofenadine hydrochloride

NDC Code 55312-571-39
Proprietary Name fexofenadine hydrochloride
Package Description 1 BOTTLE in 1 CARTON (55312-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC 55312-571
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110414
Marketing Category Name ANDA
Labeler Name Western Family Foods Inc
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of fexofenadine hydrochloride


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