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leader aller ease - 37205-650-65 - (fexofenadine hydrochloride)

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Drug Information of leader aller ease

Product NDC: 37205-650
Proprietary Name: leader aller ease
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 leader aller ease

Product NDC: 37205-650
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20110516

Package Information of leader aller ease

Package NDC: 37205-650-65
Package Description: 1 BOTTLE in 1 CARTON (37205-650-65) > 30 TABLET, FILM COATED in 1 BOTTLE

NDC Information of leader aller ease

NDC Code 37205-650-65
Proprietary Name leader aller ease
Package Description 1 BOTTLE in 1 CARTON (37205-650-65) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC 37205-650
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110516
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of leader aller ease


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