| NDC Code | 70710-1328-5 |
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| Package Description | 500 TABLET in 1 BOTTLE (70710-1328-5) |
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| Product NDC | 70710-1328 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Oxycodone And Acetaminophen |
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| Non-Proprietary Name | Oxycodone And Acetaminophen |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20171228 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210079 |
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| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
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| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
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| Strength | 325; 5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
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| DEA Schedule | CII |
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