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Fexofenadine Hydrochloride - 0904-5961-61 - (Fexofenadine Hydrochloride)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 0904-5961
Proprietary Name: Fexofenadine Hydrochloride
Non Proprietary Name: Fexofenadine Hydrochloride
Active Ingredient(s): 30    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: 0904-5961
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076502
Marketing Category: ANDA
Start Marketing Date: 20090610

Package Information of Fexofenadine Hydrochloride

Package NDC: 0904-5961-61
Package Description: 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-5961-61)

NDC Information of Fexofenadine Hydrochloride

NDC Code 0904-5961-61
Proprietary Name Fexofenadine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-5961-61)
Product NDC 0904-5961
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fexofenadine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090610
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 30
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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