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allergy relief - 11822-0571-4 - (fexofenadine hydrochloride)

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Drug Information of allergy relief

Product NDC: 11822-0571
Proprietary Name: allergy relief
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 allergy relief

Product NDC: 11822-0571
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20110415

Package Information of allergy relief

Package NDC: 11822-0571-4
Package Description: 1 BOTTLE in 1 CARTON (11822-0571-4) > 90 TABLET, FILM COATED in 1 BOTTLE

NDC Information of allergy relief

NDC Code 11822-0571-4
Proprietary Name allergy relief
Package Description 1 BOTTLE in 1 CARTON (11822-0571-4) > 90 TABLET, FILM COATED in 1 BOTTLE
Product NDC 11822-0571
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110415
Marketing Category Name ANDA
Labeler Name Rite Aid Corporation
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of allergy relief


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