| NDC Code | 63874-201-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63874-201-01) |
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| Product NDC | 63874-201 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Propoxyphene And Acetaminophen |
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| Non-Proprietary Name | Propoxyphene Napsylate And Acetaminophen |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20100101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074843 |
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| Manufacturer | Altura Pharmaceuticals, Inc. |
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| Substance Name | PROPOXYPHENE NAPSYLATE; ACETAMINOPHEN |
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| Strength | 100; 650 |
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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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