NDC11 55150018301
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 |
|---|---|
| 55150-0183-01 | 55150-0183 |
| 55150-0183-1 | 55150-0183 |
| 55150-183-01 | 55150-183 |
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 |
|---|---|---|---|---|---|---|
| NICARDIPINE HYDROCHLORIDE | NICARDIPINE HYDROCHLORIDE | Eugia US LLC | 9f5d3050-9cdf-404f-ac0f-72399178959f | 2023-06-23 | Warnings, Adverse reactions | 55150-183 |
| NICARDIPINE HYDROCHLORIDE | NICARDIPINE HYDROCHLORIDE | Eugia US LLC | dcd7d173-4d8e-4282-9edf-817711340e43 | 2021-10-11 | Warnings, Adverse reactions | 55150-183-01 55150-183 55150018301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.