| NDC Code | 0409-3459-07 |
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| Package Description | 10 AMPULE in 1 CARTON (0409-3459-07) > 1 mL in 1 AMPULE (0409-3459-17) |
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| Product NDC | 0409-3459 |
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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 | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20180823 |
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| End Marketing Date | 20211031 |
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| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
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| Manufacturer | Hospira, Inc. |
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| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
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| Strength | 2 |
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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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