| NDC Code | 47335-736-13 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-13) |
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| Product NDC | 47335-736 |
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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 | 20200301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078866 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | BUPROPION HYDROCHLORIDE |
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| Strength | 100 |
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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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