NDC11 71921017820
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 |
|---|---|
| 71921-0178-20 | 71921-0178 |
| 71921-178-20 | 71921-178 |
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 acetate | ABIRATERONE ACETATE | Florida Pharmaceutical Products, LLC. | b3e7f851-4132-4003-8f14-0eea21e5009c | 2023-04-28 | Warnings, Adverse reactions | 71921-178-20 71921-178 71921017820 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.