| NDC Code | 35356-091-90 |
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| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (35356-091-90) |
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| Product NDC | 35356-091 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Oxycontin |
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| Non-Proprietary Name | Oxycodone Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20110609 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020553 |
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| Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
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| Substance Name | OXYCODONE HYDROCHLORIDE |
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| Strength | 20 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
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| DEA Schedule | CII |
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