NDC11 76420062190
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 |
|---|---|
| 76420-0621-90 | 76420-0621 |
| 76420-621-90 | 76420-621 |
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 |
|---|---|---|---|---|---|---|
| Lansoprazole | LANSOPRAZOLE | Asclemed USA, Inc. | 71be1129-8562-476e-9d9b-99a21cbf52ec | 2026-03-24 | Warnings, Adverse reactions | 76420-621-90 76420-621 76420062190 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.