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Childrens Allegra Allergy - 41167-4222-2 - (fexofenadine hydrochloride)

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Drug Information of Childrens Allegra Allergy

Product NDC: 41167-4222
Proprietary Name: Childrens Allegra Allergy
Non Proprietary Name: fexofenadine hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   fexofenadine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Childrens Allegra Allergy

Product NDC: 41167-4222
Labeler Name: Chattem, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020872
Marketing Category: NDA
Start Marketing Date: 20110303

Package Information of Childrens Allegra Allergy

Package NDC: 41167-4222-2
Package Description: 1 BLISTER PACK in 1 CARTON (41167-4222-2) > 6 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Childrens Allegra Allergy

NDC Code 41167-4222-2
Proprietary Name Childrens Allegra Allergy
Package Description 1 BLISTER PACK in 1 CARTON (41167-4222-2) > 6 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 41167-4222
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110303
Marketing Category Name NDA
Labeler Name Chattem, Inc.
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Childrens Allegra Allergy


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