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Fexofenadine HCl - 68016-119-01 - (Fexofenadine HCl)

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Drug Information of Fexofenadine HCl

Product NDC: 68016-119
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: 68016-119
Labeler Name: Chain Drug Consortium, LLC (Premier Value)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079112
Marketing Category: ANDA
Start Marketing Date: 20120618

Package Information of Fexofenadine HCl

Package NDC: 68016-119-01
Package Description: 1 BOTTLE in 1 BOX (68016-119-01) > 45 TABLET in 1 BOTTLE

NDC Information of Fexofenadine HCl

NDC Code 68016-119-01
Proprietary Name Fexofenadine HCl
Package Description 1 BOTTLE in 1 BOX (68016-119-01) > 45 TABLET in 1 BOTTLE
Product NDC 68016-119
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120618
Marketing Category Name ANDA
Labeler Name Chain Drug Consortium, LLC (Premier Value)
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine HCl


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