| NDC Code | 0093-7517-31 |
|---|
| Package Description | 1 POUCH in 1 CARTON (0093-7517-31) > 1 INHALER in 1 POUCH > 60 POWDER in 1 INHALER |
|---|
| Product NDC | 0093-7517 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fluticasone Propionate And Salmeterol |
|---|
| Non-Proprietary Name | Fluticasone Propionate And Salmeterol |
|---|
| Dosage Form | POWDER |
|---|
| Usage | RESPIRATORY (INHALATION) |
|---|
| Start Marketing Date | 20220323 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA213948 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|
| Substance Name | FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE |
|---|
| Strength | 100; 50 |
|---|
| Strength Unit | ug/1; ug/1 |
|---|
| Pharmacy Classes | Adrenergic beta2-Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], beta2-Adrenergic Agonist [EPC] |
|---|