| NDC Code | 0378-0130-05 |
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| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0130-05) |
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| Product NDC | 0378-0130 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Propoxyphene Hydrochloride And Acetaminophen |
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| Non-Proprietary Name | Propoxyphene Hydrochloride And Acetaminophen |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20091130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA083978 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | PROPOXYPHENE HYDROCHLORIDE; ACETAMINOPHEN |
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| Strength | 65; 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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