Home > National Drug Code (NDC) > Fexofenadine Hydrochloride

Fexofenadine Hydrochloride - 0378-0782-93 - (fexofenadine)

Alphabetical Index


Drug Information of Fexofenadine Hydrochloride

Product NDC: 0378-0782
Proprietary Name: Fexofenadine Hydrochloride
Non Proprietary Name: fexofenadine
Active Ingredient(s): 180    mg/1 & nbsp;   fexofenadine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine Hydrochloride

Product NDC: 0378-0782
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077081
Marketing Category: ANDA
Start Marketing Date: 20110730

Package Information of Fexofenadine Hydrochloride

Package NDC: 0378-0782-93
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0782-93)

NDC Information of Fexofenadine Hydrochloride

NDC Code 0378-0782-93
Proprietary Name Fexofenadine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0782-93)
Product NDC 0378-0782
Product Type Name HUMAN OTC DRUG
Non Proprietary Name fexofenadine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110730
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine Hydrochloride


General Information