NDC11 70748027401
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 |
|---|---|
| 70748-0274-01 | 70748-0274 |
| 70748-0274-1 | 70748-0274 |
| 70748-274-01 | 70748-274 |
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 |
|---|---|---|---|---|---|---|
| Ganirelix Acetate | GANIRELIX ACETATE | Lupin Pharmaceuticals, Inc. | e50888ef-5e66-4b15-bdc3-2f6794f09246 | 2025-09-03 | Warnings, Adverse reactions | 70748-274-01 70748-274 70748027401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.