| NDC Code | 54868-3165-0 |
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| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (54868-3165-0) |
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| Product NDC | 54868-3165 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20040920 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078273 |
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| Manufacturer | Physicians Total Care, Inc. |
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| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
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| Strength | 2 |
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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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