| NDC Code | 0172-6359-70 |
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| Package Description | 500 TABLET, COATED in 1 BOTTLE (0172-6359-70) |
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| Product NDC | 0172-6359 |
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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, COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20050415 |
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| End Marketing Date | 20141031 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021123 |
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| Manufacturer | IVAX Pharmaceuticals, Inc. |
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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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