Etomidate
- Product NDC
- 23155-160
- 11-digit product format
- 231550160
- Labeler code
- 23155
- Product ID
- 23155-160_2a760768-0a79-426e-b7dd-ac66a9484905
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etomidate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA204618
- Marketing category
- ANDA
- Marketing start
- 2020-11-05
- 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 |
|---|
| 23155-160-41 | 23155016041 | 10 VIAL in 1 CARTON (23155-160-41) > 10 mL in 1 VIAL (23155-160-31) | 10 vial | 2020-11-05 | 0000-00-00 | No | No | Current |
| 23155-160-42 | 23155016042 | 10 VIAL in 1 CARTON (23155-160-42) > 20 mL in 1 VIAL (23155-160-32) | 10 vial | 2020-11-05 | 0000-00-00 | No | No | Current |