Product NDC: | 68788-9678 |
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: | 68788-9678 |
Labeler Name: | Preferred Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077538 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130422 |
Package NDC: | 68788-9678-1 |
Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (68788-9678-1) > 120 SPRAY, METERED in 1 BOTTLE, SPRAY |
NDC Code | 68788-9678-1 |
Proprietary Name | Fluticasone Propionate |
Package Description | 1 BOTTLE, SPRAY in 1 CARTON (68788-9678-1) > 120 SPRAY, METERED in 1 BOTTLE, SPRAY |
Product NDC | 68788-9678 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluticasone Propionate |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20130422 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc. |
Substance Name | FLUTICASONE PROPIONATE |
Strength Number | 50 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |