NDC 80830-2467-01 - Iohexol
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
- 80830-2467
- Requested NDC
- 80830-2467-01
- Package NDCs from labels
- 80830-2467-1, 80830-2467-2, 80830-2467-01
- Manufacturer
- Amneal Pharmaceuticals Private Limited
- Effective date
- 2026-06-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Iohexol - Amneal Pharmaceuticals Private Limited | Amneal Pharmaceuticals Private Limited | 2026-06-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80830-2467-1 | Iohexol | 75 mL in 1 BOTTLE, PLASTIC | INJECTION, SOLUTION | 75 | 9 | |
| 80830-2467-2 | Iohexol | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | 9 |
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 |
|---|---|---|---|---|---|---|
| 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.