# Levetiracetam

NDC: 55150-248
Generic name: Levetiracetam in sodium chloride
Labeler / Manufacturer: Eugia US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20170104

FDA application: ANDA207160

## Active ingredients

- LEVETIRACETAM: 1500 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55150-248"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55150-248
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5eb4c89-8ee9-4474-9cb1-c3b3dc262a4a