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Fexofenadine HCl - 63941-189-30 - (Fexofenadine HCl)

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Drug Information of Fexofenadine HCl

Product NDC: 63941-189
Proprietary Name: Fexofenadine HCl
Non Proprietary Name: Fexofenadine HCl
Active Ingredient(s): 180    mg/1 & nbsp;   Fexofenadine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine HCl

Product NDC: 63941-189
Labeler Name: Valu Merchandisers Company (Best Choice)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079112
Marketing Category: ANDA
Start Marketing Date: 20120604

Package Information of Fexofenadine HCl

Package NDC: 63941-189-30
Package Description: 1 BOTTLE in 1 BOX (63941-189-30) > 30 TABLET in 1 BOTTLE

NDC Information of Fexofenadine HCl

NDC Code 63941-189-30
Proprietary Name Fexofenadine HCl
Package Description 1 BOTTLE in 1 BOX (63941-189-30) > 30 TABLET in 1 BOTTLE
Product NDC 63941-189
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120604
Marketing Category Name ANDA
Labeler Name Valu Merchandisers Company (Best Choice)
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine HCl


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