NDC 70860-652-41 - Etomidate
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70860-652
- Requested NDC
- 70860-652-41
- Package NDCs from labels
- 70860-652-41, 70860-652-10, 70860-652-42, 70860-652-20
- Manufacturer
- Athenex Pharmaceutical Division, LLC.
- Effective date
- 2019-05-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Etomidate Injection, USP (2 mg per mL) (For Intravenous Use Only) | Athenex Pharmaceutical Division, LLC. | 2019-05-11 | HUMAN PRESCRIPTION DRUG LABEL |
| Etomidate Injection, USP (2 mg per mL) (For Intravenous Use Only) | REMEDYREPACK INC. | 2018-02-06 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70860-652-10 | ML - Milliliter | 70860-652 | d6bad501-7eaa-4eb8-9aac-c646909012ba | 1 | 2018-01-12 |
| 70860-652-20 | ML - Milliliter | 70860-652 | 88dca211-97c1-4ad1-869b-1156504de4cc | 1 | 2018-01-12 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Etomidate | ETOMIDATE INJECTION | Gland Pharma Limited | 94cde4e7-3b46-419f-8dda-87675da8d89d | 2017-10-17 | Warnings, Adverse reactions | ANDA209058 Z22628B598 |
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.