| NDC Code | 47335-756-52 |
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| Package Description | 12 POUCH in 1 CARTON (47335-756-52) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL |
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| Product NDC | 47335-756 |
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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 | 20211115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207875 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | ALBUTEROL SULFATE; IPRATROPIUM BROMIDE |
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| Strength | 2.5; .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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