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Fexofenadine Hydrochloride - 66336-560-30 - (Fexofenadine HCl)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 66336-560
Proprietary Name: Fexofenadine Hydrochloride
Non Proprietary Name: Fexofenadine HCl
Active Ingredient(s): 60    mg/1 & nbsp;   Fexofenadine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine Hydrochloride

Product NDC: 66336-560
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20110808

Package Information of Fexofenadine Hydrochloride

Package NDC: 66336-560-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (66336-560-30)

NDC Information of Fexofenadine Hydrochloride

NDC Code 66336-560-30
Proprietary Name Fexofenadine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (66336-560-30)
Product NDC 66336-560
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110808
Marketing Category Name ANDA
Labeler Name Dispensing Solutions, Inc.
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fexofenadine Hydrochloride


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