Product NDC: | 0054-3270 |
Proprietary Name: | Fluticasone Propionate |
Non Proprietary Name: | Fluticasone Propionate |
Active Ingredient(s): | 50 ug/1 & nbsp; Fluticasone Propionate |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-3270 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076504 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060222 |
Package NDC: | 0054-3270-99 |
Package Description: | 1 BOTTLE, GLASS in 1 CARTON (0054-3270-99) > 120 SPRAY, METERED in 1 BOTTLE, GLASS |
NDC Code | 0054-3270-99 |
Proprietary Name | Fluticasone Propionate |
Package Description | 1 BOTTLE, GLASS in 1 CARTON (0054-3270-99) > 120 SPRAY, METERED in 1 BOTTLE, GLASS |
Product NDC | 0054-3270 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluticasone Propionate |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20060222 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | FLUTICASONE PROPIONATE |
Strength Number | 50 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |