FDA NDC Directory · JSON-LD · Markdown

AMIDATE(TM) ETOMIDATE

NDC 51662-1459 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryNew Drug Application (innovator) · App NDA018227
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsETOMIDATE (2 mg/mL)
Marketing started20200331
Package count1

External sources

Source: openFDA. Public-domain (CC0).