| NDC Code | 49999-767-20 |
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| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-767-20) |
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| Product NDC | 49999-767 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Propoxyphene Napsylate 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 | 20110125 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074119 |
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| Manufacturer | Lake Erie Medical DBA Quality Care Products |
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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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