Etomidate
- Product NDC
- 70518-3203
- 11-digit product format
- 705183203
- Labeler code
- 70518
- Product ID
- 70518-3203_ca8d08c9-7101-253a-e053-2a95a90ae495
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etomidate Injection
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209058
- Marketing category
- ANDA
- Marketing start
- 2021-08-27
- 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
- 2022-12-31
- 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 |
|---|
| 70518-3203-0 | 70518320300 | 10 VIAL in 1 CARTON (70518-3203-0) > 10 mL in 1 VIAL | 10 vial | 2021-08-27 | 0000-00-00 | No | No | Current |