| NDC Code | 17856-1295-1 |
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| Package Description | 15 mL in 1 CUP (17856-1295-1) |
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| Product NDC | 17856-1295 |
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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 | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20031030 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040520 |
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| Manufacturer | Atlantic Biologicals Corps |
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| Substance Name | HYDROCODONE BITARTRATE; ACETAMINOPHEN |
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| Strength | 7.5; 500 |
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| Strength Unit | mg/15mL; mg/15mL |
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| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
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| DEA Schedule | CIII |
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