FLOVENT - 0173-0601-00 - (fluticasone propionate)

Alphabetical Index


Drug Information of FLOVENT

Product NDC: 0173-0601
Proprietary Name: FLOVENT
Non Proprietary Name: fluticasone propionate
Active Ingredient(s): 250    ug/1 & nbsp;   fluticasone propionate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): POWDER, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of FLOVENT

Product NDC: 0173-0601
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020833
Marketing Category: NDA
Start Marketing Date: 20081013

Package Information of FLOVENT

Package NDC: 0173-0601-00
Package Description: 28 POWDER, METERED in 1 INHALER (0173-0601-00)

NDC Information of FLOVENT

NDC Code 0173-0601-00
Proprietary Name FLOVENT
Package Description 28 POWDER, METERED in 1 INHALER (0173-0601-00)
Product NDC 0173-0601
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluticasone propionate
Dosage Form Name POWDER, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20081013
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name FLUTICASONE PROPIONATE
Strength Number 250
Strength Unit ug/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of FLOVENT


General Information