| NDC Code | 63739-450-10 |
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| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-450-10) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 63739-450 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Bupropion Hydrochloride |
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| Non-Proprietary Name | Bupropion Hydrochloride |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20100331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077285 |
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| Manufacturer | McKesson Packaging Services a Business unit of McKesson Corporation |
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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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