FDA NDC Directory · JSON-LD · Markdown

ETOMIDATE

NDC 51662-1485 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA202354
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsETOMIDATE (2 mg/mL)
Marketing started20200111
Package count1

External sources

Source: openFDA. Public-domain (CC0).