| NDC Code | 0785-1122-50 |
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| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (0785-1122-50) |
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| Product NDC | 0785-1122 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lorcet Plus |
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| Non-Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19841231 |
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| End Marketing Date | 20140627 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089689 |
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| Manufacturer | Forest Laboratories, Inc. |
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| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
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| Strength | 650; 7.5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
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| DEA Schedule | CIII |
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