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wal fex allergy - 0363-0571-75 - (fexofenadine hydrochloride)

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Drug Information of wal fex allergy

Product NDC: 0363-0571
Proprietary Name: wal fex allergy
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 wal fex allergy

Product NDC: 0363-0571
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20110414

Package Information of wal fex allergy

Package NDC: 0363-0571-75
Package Description: 1 BOTTLE in 1 CARTON (0363-0571-75) > 90 TABLET, FILM COATED in 1 BOTTLE

NDC Information of wal fex allergy

NDC Code 0363-0571-75
Proprietary Name wal fex allergy
Package Description 1 BOTTLE in 1 CARTON (0363-0571-75) > 90 TABLET, FILM COATED in 1 BOTTLE
Product NDC 0363-0571
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 Walgreen Company
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of wal fex allergy


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