FLOVENT - 49999-614-01 - (fluticasone propionate)

Alphabetical Index


Drug Information of FLOVENT

Product NDC: 49999-614
Proprietary Name: FLOVENT
Non Proprietary Name: fluticasone propionate
Active Ingredient(s): 110    ug/1 & nbsp;   fluticasone propionate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): AEROSOL, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of FLOVENT

Product NDC: 49999-614
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021433
Marketing Category: NDA
Start Marketing Date: 20070129

Package Information of FLOVENT

Package NDC: 49999-614-01
Package Description: 120 AEROSOL, METERED in 1 INHALER (49999-614-01)

NDC Information of FLOVENT

NDC Code 49999-614-01
Proprietary Name FLOVENT
Package Description 120 AEROSOL, METERED in 1 INHALER (49999-614-01)
Product NDC 49999-614
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluticasone propionate
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20070129
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name FLUTICASONE PROPIONATE
Strength Number 110
Strength Unit ug/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of FLOVENT


General Information