NDC11 73336007590
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 |
|---|---|
| 73336-0075-90 | 73336-0075 |
| 73336-075-90 | 73336-075 |
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 |
|---|---|---|---|---|---|---|
| GEMTESA | VIBEGRON | Sumitomo Pharma America, Inc. | 25f21d25-14f8-4fda-91f6-7aa8b68aa1c8 | 2025-04-01 | Warnings, Adverse reactions | 73336-075-90 73336-075 73336007590 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.