VERAMYST - 0173-0753-00 - (fluticasone furoate)

Alphabetical Index


Drug Information of VERAMYST

Product NDC: 0173-0753
Proprietary Name: VERAMYST
Non Proprietary Name: fluticasone furoate
Active Ingredient(s): 27.5    ug/1 & nbsp;   fluticasone furoate
Administration Route(s): NASAL
Dosage Form(s): SPRAY, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of VERAMYST

Product NDC: 0173-0753
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022051
Marketing Category: NDA
Start Marketing Date: 20070515

Package Information of VERAMYST

Package NDC: 0173-0753-00
Package Description: 120 SPRAY, METERED in 1 BOTTLE, PUMP (0173-0753-00)

NDC Information of VERAMYST

NDC Code 0173-0753-00
Proprietary Name VERAMYST
Package Description 120 SPRAY, METERED in 1 BOTTLE, PUMP (0173-0753-00)
Product NDC 0173-0753
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluticasone furoate
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20070515
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name FLUTICASONE FUROATE
Strength Number 27.5
Strength Unit ug/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of VERAMYST


General Information