| NDC Code | 35356-561-90 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (35356-561-90) |
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| Product NDC | 35356-561 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Oxycodone Hydrochloride And Ibuprofen |
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| Non-Proprietary Name | Oxycodone Hydrochloride And Ibuprofen |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20081104 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078769 |
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| Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
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| Substance Name | OXYCODONE HYDROCHLORIDE; IBUPROFEN |
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| Strength | 5; 400 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
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| DEA Schedule | CII |
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