# AMIDATE(TM) ETOMIDATE

NDC: 51662-1459
Generic name: AMIDATE(TM) ETOMIDATE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200331

FDA application: NDA018227

## Active ingredients

- ETOMIDATE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1459"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1459
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a227d2f1-3eef-4ac6-e053-2995a90a5340