NDC11 72789021398
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 |
|---|---|
| 72789-0213-98 | 72789-0213 |
| 72789-213-98 | 72789-213 |
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 |
|---|---|---|---|---|---|---|
| Abiraterone | ABIRATERONE ACETATE | PD-Rx Pharmaceuticals, Inc. | 413c645e-074d-4276-b39a-d83521077602 | 2025-10-08 | Warnings, Adverse reactions | 72789-213-98 72789-213 72789021398 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.