# Zarontin

NDC: 0071-2418
Generic name: Ethosuximide
Labeler / Manufacturer: Parke-Davis Div of Pfizer Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20200310

FDA application: ANDA080258

## Active ingredients

- ETHOSUXIMIDE: 250 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0071-2418"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0071-2418
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7bf3e616-45e8-4469-a75d-4d824ce951ea