Home > National Drug Code (NDC) > Fluticasone Propionate

Fluticasone Propionate - 50436-9992-1 - (Fluticasone Propionate)

Alphabetical Index


Drug Information of Fluticasone Propionate

Product NDC: 50436-9992
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: 50436-9992
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077570
Marketing Category: ANDA
Start Marketing Date: 20080116

Package Information of Fluticasone Propionate

Package NDC: 50436-9992-1
Package Description: 16 g in 1 BOTTLE (50436-9992-1)

NDC Information of Fluticasone Propionate

NDC Code 50436-9992-1
Proprietary Name Fluticasone Propionate
Package Description 16 g in 1 BOTTLE (50436-9992-1)
Product NDC 50436-9992
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluticasone Propionate
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20080116
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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