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Fexofenadine Hydrochloride - 54868-5409-0 - (Fexofenadine Hydrochloride)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 54868-5409
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine Hydrochloride

Product NDC: 54868-5409
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA020872
Marketing Category: ANDA
Start Marketing Date: 20070404

Package Information of Fexofenadine Hydrochloride

Package NDC: 54868-5409-0
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (54868-5409-0)

NDC Information of Fexofenadine Hydrochloride

NDC Code 54868-5409-0
Proprietary Name Fexofenadine Hydrochloride
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (54868-5409-0)
Product NDC 54868-5409
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fexofenadine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070404
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Fexofenadine Hydrochloride


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