| NDC Code | 0603-4186-32 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-4186-32) |
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| Product NDC | 0603-4186 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Levetiracetam |
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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 | 20120720 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202533 |
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| Manufacturer | Qualitest Pharmaceuticals |
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| Substance Name | LEVETIRACETAM |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
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