# Levetiracetam

NDC: 70069-846
Generic name: Levetiracetam in Sodium Chloride
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260420

FDA application: ANDA219562

## Active ingredients

- LEVETIRACETAM: 1000 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-846"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-846
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b37c579-ebe7-4ce1-8a34-03e974a77439