Home > National Drug Code (NDC) > Fexofenadine Hydrochloride

Fexofenadine Hydrochloride - 51079-526-20 - (fexofenadine hydrochloride)

Alphabetical Index


Drug Information of Fexofenadine Hydrochloride

Product NDC: 51079-526
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: 51079-526
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077081
Marketing Category: ANDA
Start Marketing Date: 20100521

Package Information of Fexofenadine Hydrochloride

Package NDC: 51079-526-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-526-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-526-01)

NDC Information of Fexofenadine Hydrochloride

NDC Code 51079-526-20
Proprietary Name Fexofenadine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-526-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-526-01)
Product NDC 51079-526
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fexofenadine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100521
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
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


General Information