NDC11 57483090042
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 |
|---|---|
| 57483-0900-42 | 57483-0900 |
| 57483-900-42 | 57483-900 |
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 |
|---|---|---|---|---|---|---|
| Esomeprazole | ESOMEPRAZOLE MAGNESIUM | INNOVUS PHARMACEUTICALS, INC. | b3d10f0b-52af-408c-9b3d-f8f25f7c42bd | 2024-10-30 | Warnings | 57483-900-42 57483-900 57483090042 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.