NDC11 51991075990
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 |
|---|---|
| 51991-0759-90 | 51991-0759 |
| 51991-759-90 | 51991-759 |
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 |
|---|---|---|---|---|---|---|
| LETROZOLE | LETROZOLE | Breckenridge Pharmaceutical, Inc. | 63e54b62-a30d-4a56-9215-75e7a0b0bf02 | 2026-08-17 | Warnings, Adverse reactions | 51991-759-90 51991-759 51991075990 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.