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Allegra--D 24 Hour - 54868-5419-0 - (fexofenadine hydrochloride and pseudoephedrine hydrochloride)

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Drug Information of Allegra--D 24 Hour

Product NDC: 54868-5419
Proprietary Name: Allegra--D 24 Hour
Non Proprietary Name: fexofenadine hydrochloride and pseudoephedrine hydrochloride
Active Ingredient(s): 180; 240    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 24 Hour

Product NDC: 54868-5419
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021704
Marketing Category: NDA
Start Marketing Date: 20050914

Package Information of Allegra--D 24 Hour

Package NDC: 54868-5419-0
Package Description: 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5419-0)

NDC Information of Allegra--D 24 Hour

NDC Code 54868-5419-0
Proprietary Name Allegra--D 24 Hour
Package Description 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5419-0)
Product NDC 54868-5419
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fexofenadine hydrochloride and pseudoephedrine hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20050914
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 180; 240
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 24 Hour


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