| NDC Code | 51672-4258-1 |
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| Package Description | 1 BOTTLE in 1 CARTON (51672-4258-1) / 216 TABLET in 1 BOTTLE |
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| Product NDC | 51672-4258 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Acetaminophen 250 Mg And Ibuprofen 125 Mg |
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| Non-Proprietary Name | Acetaminophen 250 Mg And Ibuprofen 125 Mg Tablets |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20260315 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA219053 |
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| Manufacturer | Sun Pharmaceutical Industries, 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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