NDC11 73159000860
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 |
|---|---|
| 73159-0008-60 | 73159-0008 |
| 73159-008-60 | 73159-008 |
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 |
|---|---|---|---|---|---|---|
| ULTRAVATE | HALOBETASOL PROPIONATE | Lacer Pharma, LLC | 74e899db-1c1f-48b2-9913-5d32a14906ae | 2025-04-06 | Warnings, Adverse reactions | 73159-008-60 73159-008 73159000860 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.