| NDC Code | 66336-897-30 |
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| Package Description | 30 TABLET in 1 BOTTLE (66336-897-30) |
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| Product NDC | 66336-897 |
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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 |
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| Usage | OCCLUSIVE DRESSING TECHNIQUE |
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| Start Marketing Date | 20080312 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077455 |
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| Manufacturer | Dispensing Solutions, Inc. |
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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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