NDC11 59651032905
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 |
|---|---|
| 59651-0329-05 | 59651-0329 |
| 59651-0329-5 | 59651-0329 |
| 59651-329-05 | 59651-329 |
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 |
|---|---|---|---|---|---|---|
| Montelukast Sodium | MONTELUKAST SODIUM | Aurobindo Pharma Limited | 9a3bfc59-0ca6-4433-abf5-41659bfe0a8f | 2023-06-03 | Boxed warning, Warnings, Adverse reactions | 59651-329-05 59651-329 59651032905 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.