NDC11 76420027001
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 |
|---|---|
| 76420-0270-01 | 76420-0270 |
| 76420-0270-1 | 76420-0270 |
| 76420-270-01 | 76420-270 |
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 |
|---|---|---|---|---|---|---|
| DMT SUIK | DEXAMETHASONE SODIUM PHOSPHATE | Asclemed USA, Inc. | a7b7884a-6bd4-4d06-8f14-0759450c0724 | 2020-06-17 | Warnings, Adverse reactions | 76420-270-01 76420-270 76420027001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.