| NDC Code | 50844-598-14 |
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| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-598-14) |
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| Product NDC | 50844-598 |
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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, Ibuprofen |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20260910 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA220126 |
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| Manufacturer | L.N.K. International, 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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