| NDC Code | 60687-148-21 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-148-21) > 1 TABLET in 1 BLISTER PACK (60687-148-11) |
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| Product NDC | 60687-148 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Oxymorphone Hydrochloride |
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| Non-Proprietary Name | Oxymorphone Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20151201 |
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| End Marketing Date | 20180930 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021611 |
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| Manufacturer | American Health Packaging |
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| Substance Name | OXYMORPHONE HYDROCHLORIDE |
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| Strength | 10 |
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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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