FDA NDC Directory · JSON-LD · Markdown

ETOMIDATE

NDC 55150-222 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerEugia US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206126
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsETOMIDATE (40 mg/20mL)
Marketing started20170224
Package count1

External sources

Source: openFDA. Public-domain (CC0).