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Fexofenadine Hydrochloride - 0904-6311-89 - (Fexofenadine HCl)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 0904-6311
Proprietary Name: Fexofenadine Hydrochloride
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 Hydrochloride

Product NDC: 0904-6311
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079112
Marketing Category: ANDA
Start Marketing Date: 20120904

Package Information of Fexofenadine Hydrochloride

Package NDC: 0904-6311-89
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (0904-6311-89)

NDC Information of Fexofenadine Hydrochloride

NDC Code 0904-6311-89
Proprietary Name Fexofenadine Hydrochloride
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (0904-6311-89)
Product NDC 0904-6311
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120904
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine Hydrochloride


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