| NDC Code | 0093-3607-82 |
|---|
| Package Description | 1 POUCH in 1 CARTON (0093-3607-82) / 1 INHALER in 1 POUCH / 60 POWDER, METERED in 1 INHALER |
|---|
| Product NDC | 0093-3607 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fluticasone Propionate And Salmeterol |
|---|
| Non-Proprietary Name | Fluticasone Propionate And Salmeterol |
|---|
| Dosage Form | POWDER, METERED |
|---|
| Usage | RESPIRATORY (INHALATION) |
|---|
| Start Marketing Date | 20170428 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA208799 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|
| Substance Name | FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE |
|---|
| Strength | 55; 14 |
|---|
| Strength Unit | ug/1; ug/1 |
|---|
| Pharmacy Classes | Adrenergic beta2-Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], beta2-Adrenergic Agonist [EPC] |
|---|