| NDC Code | 70518-3968-0 |
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| Package Description | 1 POUCH in 1 CARTON (70518-3968-0) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALER |
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| Product NDC | 70518-3968 |
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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 |
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| Usage | RESPIRATORY (INHALATION) |
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| Start Marketing Date | 20231226 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203433 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE |
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| Strength | 250; 50 |
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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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