Etomidate
- Product NDC
- 70860-652
- 11-digit product format
- 708600652
- Labeler code
- 70860
- Product ID
- 70860-652_9b3038c5-99ad-4a96-87c2-c5c68389bd73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- etomidate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA209058
- Marketing category
- ANDA
- Marketing start
- 2017-08-01
- 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
- 2020-12-31
- 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 |
|---|
| 70860-652-10 | 70860065210 | 10 VIAL in 1 CARTON (70860-652-10) > 10 mL in 1 VIAL (70860-652-41) | 10 vial | 2017-08-01 | 0000-00-00 | No | No | Current |
| 70860-652-20 | 70860065220 | 10 VIAL in 1 CARTON (70860-652-20) > 20 mL in 1 VIAL (70860-652-42) | 10 vial | 2017-08-01 | 0000-00-00 | No | No | Current |