| NDC Code | 70518-2250-1 |
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| Package Description | 5 POUCH in 1 CARTON (70518-2250-1) / 6 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 70518-2250 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ipratropium Bromide And Albuterol Sulfate |
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| Non-Proprietary Name | Ipratropium Bromide And Albuterol Sulfate |
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| Dosage Form | SOLUTION |
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| Usage | RESPIRATORY (INHALATION) |
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| Start Marketing Date | 20190802 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076749 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | ALBUTEROL SULFATE; IPRATROPIUM BROMIDE |
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| Strength | 3; .5 |
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| Strength Unit | mg/3mL; mg/3mL |
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| Pharmacy Classes | Adrenergic beta2-Agonists [MoA], Anticholinergic [EPC], Cholinergic Antagonists [MoA], beta2-Adrenergic Agonist [EPC] |
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