| NDC Code | 65084-444-32 |
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| Package Description | 180 TABLET in 1 BOTTLE (65084-444-32) |
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| Product NDC | 65084-444 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Non-Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20100913 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089160 |
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| Manufacturer | Rx Pak Division of McKesson Corporation |
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| Substance Name | HYDROCODONE BITARTRATE; ACETAMINOPHEN |
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| Strength | 5; 500 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
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| DEA Schedule | CIII |
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