NDC11 24208072002
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 |
|---|---|
| 24208-0720-02 | 24208-0720 |
| 24208-0720-2 | 24208-0720 |
| 24208-720-02 | 24208-720 |
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 |
|---|---|---|---|---|---|---|
| Dexamethasone Sodium Phosphate | DEXAMETHASONE SODIUM PHOSPHATE | Bausch & Lomb Incorporated | 6bdcefbe-51e3-4ca4-afda-5aeca7b6fa73 | 2022-08-31 | Warnings, Adverse reactions | 24208-720-02 24208-720 24208072002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.