# LEVETIRACETAM Extended-release

NDC: 81665-101
Generic name: LEVETIRACETAM
Labeler / Manufacturer: Omnivium Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230505

FDA application: ANDA212688

## Active ingredients

- LEVETIRACETAM: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81665-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81665-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a31134d-6b63-4d14-8445-0ed132e6c88d