| NDC Code | 42858-302-50 |
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| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (42858-302-50) |
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| Product NDC | 42858-302 |
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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 | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20091123 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA019892 |
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| Manufacturer | Rhodes Pharmaceuticals L.P. |
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| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
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| Strength | 4 |
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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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