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Allegra D-12 Hour - 0088-1090-49 - (fexofenadine hydrochloride and pseudoephedrine hydrochloride)

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Drug Information of Allegra D-12 Hour

Product NDC: 0088-1090
Proprietary Name: Allegra D-12 Hour
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Allegra D-12 Hour

Product NDC: 0088-1090
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020786
Marketing Category: NDA
Start Marketing Date: 19971224

Package Information of Allegra D-12 Hour

Package NDC: 0088-1090-49
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0088-1090-49)

NDC Information of Allegra D-12 Hour

NDC Code 0088-1090-49
Proprietary Name Allegra D-12 Hour
Package Description 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0088-1090-49)
Product NDC 0088-1090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fexofenadine hydrochloride and pseudoephedrine hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19971224
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 60; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of Allegra D-12 Hour


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