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Allegra D 12 Hour Allergy and Congestion - 21695-931-20 - (fexofenadine hydrochloride and pseudoephedrine hydrochloride)

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Drug Information of Allegra D 12 Hour Allergy and Congestion

Product NDC: 21695-931
Proprietary Name: Allegra D 12 Hour Allergy and Congestion
Non Proprietary Name: fexofenadine hydrochloride and pseudoephedrine hydrochloride
Active Ingredient(s): 60; 120    mg/1; mg/1 & nbsp;   fexofenadine hydrochloride and pseudoephedrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Allegra D 12 Hour Allergy and Congestion

Product NDC: 21695-931
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020786
Marketing Category: NDA
Start Marketing Date: 20110303

Package Information of Allegra D 12 Hour Allergy and Congestion

Package NDC: 21695-931-20
Package Description: 4 BLISTER PACK in 1 CARTON (21695-931-20) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Allegra D 12 Hour Allergy and Congestion

NDC Code 21695-931-20
Proprietary Name Allegra D 12 Hour Allergy and Congestion
Package Description 4 BLISTER PACK in 1 CARTON (21695-931-20) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 21695-931
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine hydrochloride and pseudoephedrine hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110303
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 60; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Allegra D 12 Hour Allergy and Congestion


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