| NDC Code | 50228-190-05 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-190-05) |
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| Product NDC | 50228-190 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Levetiracetam |
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| Proprietary Name Suffix | Extended-release |
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| Non-Proprietary Name | Levetiracetam |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20201127 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205130 |
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| Manufacturer | ScieGen Pharmaceuticals, Inc |
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| Substance Name | LEVETIRACETAM |
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| Strength | 750 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Decreased Central Nervous System Disorganized Electrical Activity [PE] |
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