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Fexofenadine Hydrochloride - 63629-3190-4 - (Fexofenadine Hydrochloride)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 63629-3190
Proprietary Name: Fexofenadine Hydrochloride
Non Proprietary Name: Fexofenadine Hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   Fexofenadine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine Hydrochloride

Product NDC: 63629-3190
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076502
Marketing Category: ANDA
Start Marketing Date: 20060412

Package Information of Fexofenadine Hydrochloride

Package NDC: 63629-3190-4
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (63629-3190-4)

NDC Information of Fexofenadine Hydrochloride

NDC Code 63629-3190-4
Proprietary Name Fexofenadine Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (63629-3190-4)
Product NDC 63629-3190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fexofenadine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060412
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Fexofenadine Hydrochloride


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