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