ALLEGRA - 0088-1097-20 - (fexofenadine hydrochloride)

Alphabetical Index


Drug Information of ALLEGRA

Product NDC: 0088-1097
Proprietary Name: ALLEGRA
Non Proprietary Name: fexofenadine hydrochloride
Active Ingredient(s): 6    mg/mL & nbsp;   fexofenadine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of ALLEGRA

Product NDC: 0088-1097
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021963
Marketing Category: NDA
Start Marketing Date: 20061016

Package Information of ALLEGRA

Package NDC: 0088-1097-20
Package Description: 300 mL in 1 BOTTLE (0088-1097-20)

NDC Information of ALLEGRA

NDC Code 0088-1097-20
Proprietary Name ALLEGRA
Package Description 300 mL in 1 BOTTLE (0088-1097-20)
Product NDC 0088-1097
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fexofenadine hydrochloride
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20061016
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 6
Strength Unit mg/mL
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of ALLEGRA


General Information