| NDC Code | 47335-576-88 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-576-88) |
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| Product NDC | 47335-576 |
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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 | 20130909 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203059 |
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| Manufacturer | Sun Pharmaceutical Industries, 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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