NDC11 51991062090
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 |
|---|---|
| 51991-0620-90 | 51991-0620 |
| 51991-620-90 | 51991-620 |
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 |
|---|---|---|---|---|---|---|
| ANASTROZOLE | ANASTROZOLE | Breckenridge Pharmaceutical, Inc. | ca9d4aff-ffdf-4a46-ad20-e47e5886a19e | 2026-08-18 | Warnings, Adverse reactions | 51991-620-90 51991-620 51991062090 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.