ETOMIDATE
- Product NDC
- 55150-222
- 11-digit product format
- 551500222
- Labeler code
- 55150
- Product ID
- 55150-222_278b160e-cdc4-451e-9405-cb001f443680
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ETOMIDATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Eugia US LLC
- Application
- ANDA206126
- Marketing category
- ANDA
- Marketing start
- 2017-02-24
- Substance
- ETOMIDATE
- Active strength
- 40 mg/20mL
- Pharmacologic classes
- General Anesthesia [PE], General Anesthetic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ETOMIDATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ETOMIDATE | 40 mg/20mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Z22628B598 |
| Rxcui | 1654006, 1654008 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55150-222-20 | ETOMIDATE | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 5 |
| 55150-222-20 | ETOMIDATE | 20 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 20 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55150-222 | ETOMIDATE INJECTION, SOLUTION [EUGIA US LLC] | 5 | Current NDC, Legacy NDC, 2 package rows | 20230707_0820f15a-046b-4185-a2b3-2e4051ee3d82.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55150-222-20 | 55150022220 | 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-222-20) / 20 mL in 1 VIAL, SINGLE-DOSE | 2017-02-24 | 0000-00-00 | No | No | Current |