| NDC Code | 11014-0104-1 |
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| Package Description | 1 BAG in 1 CONTAINER (11014-0104-1) > 1865149 TABLET, FILM COATED, EXTENDED RELEASE in 1 BAG |
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| Product NDC | 11014-0104 |
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| Product Type Name | BULK INGREDIENT |
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| Non-Proprietary Name | Bupropion Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Start Marketing Date | 20100719 |
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| End Marketing Date | 20161025 |
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| Marketing Category Name | DRUG FOR FURTHER PROCESSING |
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| Manufacturer | Catalent Pharma Solutions, LLC |
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| Substance Name | BUPROPION HYDROCHLORIDE |
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| Strength | 200 |
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| Strength Unit | mg/1 |
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