# Levetiracetam

NDC: 87063-192
Generic name: Levetiracetam
Labeler / Manufacturer: ASCLEMED USA INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230501

FDA application: ANDA091491

## Active ingredients

- LEVETIRACETAM: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87063-192"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87063-192
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a3c57d82-511c-4c7d-84ff-f791f931f576