| NDC Code | 43063-023-04 |
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| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-023-04) |
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| Product NDC | 43063-023 |
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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 | 20100510 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074843 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE |
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| Strength | 650; 100 |
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| Strength Unit | 1/1; 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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