| NDC Code | 70000-0622-2 |
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| Package Description | 36 TABLET in 1 BOTTLE (70000-0622-2) |
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| Product NDC | 70000-0622 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Acetaminophen And Ibuprofen |
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| Non-Proprietary Name | Acetaminophen And Ibuprofen |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20230715 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216592 |
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| Manufacturer | LEADER/ Cardinal Health 110, Inc. |
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| Substance Name | ACETAMINOPHEN; IBUPROFEN |
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| Strength | 250; 125 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
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