| NDC Code | 43063-772-70 |
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| Package Description | 70 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-772-70) |
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| Product NDC | 43063-772 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Contrave |
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| Proprietary Name Suffix | Extended-release |
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| Non-Proprietary Name | Naltrexone Hydrochloride And Bupropion Hydrochloride |
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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 | NDA |
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| Application Number | NDA200063 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | BUPROPION HYDROCHLORIDE; NALTREXONE HYDROCHLORIDE |
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| Strength | 90; 8 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA], Opioid Antagonist [EPC], Opioid Antagonists [MoA] |
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