| NDC Code | 0591-3332-05 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3332-05) |
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| Product NDC | 0591-3332 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Bupropion Hydrochloride |
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| Proprietary Name Suffix | Xl |
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| Non-Proprietary Name | Bupropion Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20070613 |
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| End Marketing Date | 20150731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077715 |
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| Manufacturer | Actavis Pharma, Inc. |
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| Substance Name | BUPROPION HYDROCHLORIDE |
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| Strength | 300 |
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| Strength Unit | 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] |
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