# Levetiracetam

NDC: 76494-528
Generic name: Levetiracetam
Labeler / Manufacturer: Prinston Pharmaceutical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120911

FDA application: ANDA078106

## Active ingredients

- LEVETIRACETAM: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76494-528"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76494-528
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d818ef84-9b3e-434b-92d9-910cfa8af7da