Home > National Drug Code (NDC) > fexofenadine hydrochloride

fexofenadine hydrochloride - 35356-749-60 - (fexofenadine hydrochloride)

Alphabetical Index


Drug Information of fexofenadine hydrochloride

Product NDC: 35356-749
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: 35356-749
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20110414

Package Information of fexofenadine hydrochloride

Package NDC: 35356-749-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (35356-749-60)

NDC Information of fexofenadine hydrochloride

NDC Code 35356-749-60
Proprietary Name fexofenadine hydrochloride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (35356-749-60)
Product NDC 35356-749
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110414
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of fexofenadine hydrochloride


General Information