| NDC Code | 65162-617-11 |
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| Package Description | 1000 TABLET in 1 BOTTLE (65162-617-11) |
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| Product NDC | 65162-617 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tramadol Hydrochloride And Acetaminophen |
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| Non-Proprietary Name | Tramadol Hydrochloride And Acetaminophen |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20091217 |
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| End Marketing Date | 20240106 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090485 |
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| Manufacturer | Amneal Pharmaceuticals LLC |
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| Substance Name | ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
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| Strength | 325; 37.5 |
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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 | CIV |
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