# ETOMIDATE

NDC: 51662-1542
Generic name: ETOMIDATE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220409

FDA application: ANDA206126

## Active ingredients

- ETOMIDATE: 40 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1542"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1542
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc43b289-4f32-1c1e-e053-2995a90a3a23