| NDC Code | 17856-0386-1 |
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| Package Description | 72 CUP in 1 CASE (17856-0386-1) / 5 mL in 1 CUP (17856-0386-2) |
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| Product NDC | 17856-0386 |
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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 | 20120301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074653 |
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| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
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| Strength | 1 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
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| DEA Schedule | CII |
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