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Fexofenadine - 64679-987-12 - (Fexofenadine)

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Drug Information of Fexofenadine

Product NDC: 64679-987
Proprietary Name: Fexofenadine
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

Product NDC: 64679-987
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079112
Marketing Category: ANDA
Start Marketing Date: 20120208

Package Information of Fexofenadine

Package NDC: 64679-987-12
Package Description: 1 BOTTLE in 1 CARTON (64679-987-12) > 30 TABLET, FILM COATED in 1 BOTTLE

NDC Information of Fexofenadine

NDC Code 64679-987-12
Proprietary Name Fexofenadine
Package Description 1 BOTTLE in 1 CARTON (64679-987-12) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC 64679-987
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120208
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine


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