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Fexofenadine hydrochloride - 54868-6289-0 - (Fexofenadine hydrochloride)

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Drug Information of Fexofenadine hydrochloride

Product NDC: 54868-6289
Proprietary Name: Fexofenadine hydrochloride
Non Proprietary Name: Fexofenadine hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   Fexofenadine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine hydrochloride

Product NDC: 54868-6289
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076502
Marketing Category: ANDA
Start Marketing Date: 20110727

Package Information of Fexofenadine hydrochloride

Package NDC: 54868-6289-0
Package Description: 30 TABLET in 1 BOTTLE (54868-6289-0)

NDC Information of Fexofenadine hydrochloride

NDC Code 54868-6289-0
Proprietary Name Fexofenadine hydrochloride
Package Description 30 TABLET in 1 BOTTLE (54868-6289-0)
Product NDC 54868-6289
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110727
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine hydrochloride


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