# Levetiracetam in Sodium Chloride

NDC: 14789-220
Generic name: Levetiracetam
Labeler / Manufacturer: Nexus Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20200720

FDA application: ANDA213532

## Active ingredients

- LEVETIRACETAM: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"14789-220"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=14789-220
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee014183-a857-457b-9573-0cc168e560f3