| NDC Code | 13107-004-99 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (13107-004-99) |
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| Product NDC | 13107-004 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20160602 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204575 |
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| Manufacturer | Aurolife Pharma, LLC |
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| Substance Name | HYDROCODONE BITARTRATE; IBUPROFEN |
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| Strength | 7.5; 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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