| NDC Code | 52959-738-20 |
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| Package Description | 20 TABLET in 1 BOTTLE (52959-738-20) |
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| Product NDC | 52959-738 |
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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 | 20100118 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076642 |
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| Manufacturer | H.J. Harkins Company, Inc. |
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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 | Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
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| DEA Schedule | CIII |
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