FDA NDC Directory · JSON-LD · Markdown

Etomidate

NDC 68083-235 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameEtomidate Injection
Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA209058
Dosage form / routeSOLUTION · INTRAVENOUS
Active ingredientsETOMIDATE (2 mg/mL)
Marketing started20170520
Package count1

External sources

Source: openFDA. Public-domain (CC0).