United States · FDA National Drug Code directory
Amidate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0409-6695_3f83ed21-1b60-486c-8c70-1d5aa7553404
- Product NDC
- 0409-6695
- Form
- INJECTION, SOLUTION
- Composition / generic term
- ETOMIDATE
- Labeler
- Hospira, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20050726
- Source listing expiry
- 20271231
Source-listed ingredients
- ETOMIDATE — 2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6695-01) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6695-11) · 0409-6695-01
- 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6695-02) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-6695-12) · 0409-6695-02
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →