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Fexofenadine Hydrochloride - 0378-0780-05 - (fexofenadine)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 0378-0780
Proprietary Name: Fexofenadine Hydrochloride
Non Proprietary Name: fexofenadine
Active Ingredient(s): 30    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: 0378-0780
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: 0378-0780-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0780-05)

NDC Information of Fexofenadine Hydrochloride

NDC Code 0378-0780-05
Proprietary Name Fexofenadine Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0780-05)
Product NDC 0378-0780
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 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine Hydrochloride


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