| NDC Code | 60687-566-86 |
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| Package Description | 3 TRAY in 1 CASE (60687-566-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-566-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-566-40) |
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| Product NDC | 60687-566 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydromorphone Hydrochloride |
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| Non-Proprietary Name | Hydromorphone Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20210901 |
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| End Marketing Date | 20251231 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA019891 |
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| Manufacturer | American Health Packaging |
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| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
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| DEA Schedule | CII |
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