etomidate
- Product NDC
- 25021-674
- 11-digit product format
- 250210674
- Labeler code
- 25021
- Product ID
- 25021-674_53cc21c1-422a-4eee-b2d8-828148c576db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- etomidate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA215028
- Marketing category
- ANDA
- Marketing start
- 2012-08-10
- Marketing end
- 0000-00-00
- Substance
- ETOMIDATE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- General Anesthesia [PE], General Anesthetic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 25021-674-10 | 25021067410 | 10 VIAL in 1 CARTON (25021-674-10) > 10 mL in 1 VIAL | 10 vial | 2012-08-10 | 0000-00-00 | No | No | Current |
| 25021-674-20 | 25021067420 | 10 VIAL in 1 CARTON (25021-674-20) > 20 mL in 1 VIAL | 10 vial | 2012-08-10 | 0000-00-00 | No | No | Current |