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Fexofenadine - 55648-987-10 - (Fexofenadine)

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Drug Information of Fexofenadine

Product NDC: 55648-987
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: 55648-987
Labeler Name: Wockhardt Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079112
Marketing Category: ANDA
Start Marketing Date: 20120208

Package Information of Fexofenadine

Package NDC: 55648-987-10
Package Description: 1 BLISTER PACK in 1 CARTON (55648-987-10) > 5 TABLET, FILM COATED in 1 BLISTER PACK (55648-987-09)

NDC Information of Fexofenadine

NDC Code 55648-987-10
Proprietary Name Fexofenadine
Package Description 1 BLISTER PACK in 1 CARTON (55648-987-10) > 5 TABLET, FILM COATED in 1 BLISTER PACK (55648-987-09)
Product NDC 55648-987
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 Limited
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine


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