| NDC Code | 50090-3272-0 |
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| Package Description | 1 POUCH in 1 CARTON (50090-3272-0) / 1 POWDER, METERED in 1 POUCH |
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| Product NDC | 50090-3272 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fluticasone Propionate And Salmeterol |
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| Non-Proprietary Name | Fluticasone Propionate And Salmeterol |
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| Dosage Form | POWDER, METERED |
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| Usage | RESPIRATORY (INHALATION) |
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| Start Marketing Date | 20170428 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA208799 |
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| Manufacturer | A-S Medication Solutions |
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| Substance Name | FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE |
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| Strength | 55; 14 |
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| Strength Unit | ug/1; ug/1 |
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| Pharmacy Classes | Adrenergic beta2-Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], beta2-Adrenergic Agonist [EPC] |
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