| NDC Code | 63629-5437-2 |
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| Package Description | 20 TABLET in 1 BOTTLE (63629-5437-2) |
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| Product NDC | 63629-5437 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocodone Bitartrate And Ibuprofen |
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| Non-Proprietary Name | Hydrocodone Bitartrate And Ibuprofen |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20100218 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076642 |
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| Manufacturer | Bryant Ranch Prepack |
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| Substance Name | HYDROCODONE BITARTRATE; IBUPROFEN |
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| Strength | 2.5; 200 |
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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], Opioid Agonist [EPC], Opioid Agonists [MoA] |
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| DEA Schedule | CII |
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