| NDC Code | 51662-1634-1 |
| Package Description | 10 mL in 1 VIAL, SINGLE-DOSE (51662-1634-1) |
| Product NDC | 51662-1634 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Proprietary Name | Etomidate Injection, Solution |
| Non-Proprietary Name | Etomidate Injection, Solution |
| Dosage Form | INJECTION, SOLUTION |
| Usage | INTRAVENOUS |
| Start Marketing Date | 20230925 |
| Marketing Category Name | ANDA |
| Application Number | ANDA206126 |
| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
| Substance Name | ETOMIDATE |
| Strength | 20 |
| Strength Unit | mg/10mL |
| Pharmacy Classes | General Anesthesia [PE], General Anesthetic [EPC] |