NDC11 65219038305
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 65219-0383-05 | 65219-0383 |
| 65219-0383-5 | 65219-0383 |
| 65219-383-05 | 65219-383 |
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 |
|---|---|---|---|---|---|---|
| BL-C Kit | BETAMETHASONE SODIUM PHOSPHATE, BETAMETHASONE ACETATE, LIDOCAINE, IODIXANOL, POVIDINE IODINE | Asclemed USA, Inc. | 798f3bc6-d976-49a6-87a2-fd30c784fc50 | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 65219-383-05 65219038305 |
| Iodixanol | IODIXANOL | FRESENIUS KABI USA, LLC | 0fe89ea2-04f7-46c5-9c35-220d8c144a95 | 2023-07-21 | Boxed warning, Warnings, Adverse reactions | 65219-383-05 65219-383 65219038305 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.