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FEXOFENADINE HYDROCHLORIDE - 62756-542-83 - (FEXOFENADINE HYDROCHLORIDE)

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Drug Information of FEXOFENADINE HYDROCHLORIDE

Product NDC: 62756-542
Proprietary Name: FEXOFENADINE HYDROCHLORIDE
Non Proprietary Name: FEXOFENADINE HYDROCHLORIDE
Active Ingredient(s): 30    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: 62756-542
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091567
Marketing Category: ANDA
Start Marketing Date: 20120206

Package Information of FEXOFENADINE HYDROCHLORIDE

Package NDC: 62756-542-83
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (62756-542-83)

NDC Information of FEXOFENADINE HYDROCHLORIDE

NDC Code 62756-542-83
Proprietary Name FEXOFENADINE HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (62756-542-83)
Product NDC 62756-542
Product Type Name HUMAN OTC DRUG
Non Proprietary Name FEXOFENADINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120206
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of FEXOFENADINE HYDROCHLORIDE


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