| NDC Code | 0051-0629-12 |
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| Package Description | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (0051-0629-12) |
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| Product NDC | 0051-0629 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Naltrexone Hydrochloride And Bupropion Hydrochloride |
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| Proprietary Name Suffix | Extended-release |
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| Non-Proprietary Name | Naltrexone Hydrochloride And Bupropion Hydorchloride |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20141022 |
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| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
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| Application Number | NDA200063 |
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| Manufacturer | AbbVie Inc. |
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| Substance Name | NALTREXONE HYDROCHLORIDE; BUPROPION HYDROCHLORIDE |
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| Strength | 8; 90 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Opioid Antagonist [EPC],Opioid Antagonists [MoA],Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
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