| NDC Code | 53002-2666-1 |
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| Package Description | 1 POUCH in 1 CARTON (53002-2666-1) > 1 AEROSOL in 1 POUCH |
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| Product NDC | 53002-2666 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Budesonide And Formoterol Fumarate Dihydrate |
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| Non-Proprietary Name | Budesonide And Formoterol Fumarate Dihydrate |
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| Dosage Form | AEROSOL |
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| Usage | RESPIRATORY (INHALATION) |
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| Start Marketing Date | 20200103 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021929 |
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| Manufacturer | RPK Pharmaceuticals, Inc. |
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| Substance Name | BUDESONIDE; FORMOTEROL FUMARATE |
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| Strength | 80; 4.5 |
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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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