Home > National Drug Code (NDC) > Fluticasone Propionate

Fluticasone Propionate - 49999-982-16 - (Fluticasone Propionate)

Alphabetical Index


Drug Information of Fluticasone Propionate

Product NDC: 49999-982
Proprietary Name: Fluticasone Propionate
Non Proprietary Name: Fluticasone Propionate
Active Ingredient(s): 50    ug/.1g & nbsp;   Fluticasone Propionate
Administration Route(s): NASAL
Dosage Form(s): SPRAY, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of Fluticasone Propionate

Product NDC: 49999-982
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077570
Marketing Category: ANDA
Start Marketing Date: 20120312

Package Information of Fluticasone Propionate

Package NDC: 49999-982-16
Package Description: 1 BOTTLE, PUMP in 1 CARTON (49999-982-16) > 16 g in 1 BOTTLE, PUMP

NDC Information of Fluticasone Propionate

NDC Code 49999-982-16
Proprietary Name Fluticasone Propionate
Package Description 1 BOTTLE, PUMP in 1 CARTON (49999-982-16) > 16 g in 1 BOTTLE, PUMP
Product NDC 49999-982
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluticasone Propionate
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20120312
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name FLUTICASONE PROPIONATE
Strength Number 50
Strength Unit ug/.1g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Fluticasone Propionate


General Information