| NDC Code | 61919-038-72 |
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| Package Description | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-038-72) |
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| Product NDC | 61919-038 |
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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, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20140101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078866 |
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| Manufacturer | DIRECT RX |
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| Substance Name | BUPROPION HYDROCHLORIDE |
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| Strength | 150 |
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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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