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Fexofenadine Hydrochloride - 0615-5619-39 - (Fexofenadine Hydrochloride)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 0615-5619
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: 0615-5619
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020872
Marketing Category: NDA
Start Marketing Date: 20000225

Package Information of Fexofenadine Hydrochloride

Package NDC: 0615-5619-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-5619-39)

NDC Information of Fexofenadine Hydrochloride

NDC Code 0615-5619-39
Proprietary Name Fexofenadine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-5619-39)
Product NDC 0615-5619
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fexofenadine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000225
Marketing Category Name NDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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