NDC11 65219002805
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 |
|---|---|
| 65219-0028-05 | 65219-0028 |
| 65219-0028-5 | 65219-0028 |
| 65219-028-05 | 65219-028 |
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 | Fresenius Kabi USA, LLC | c23ca7b2-7350-4f07-8adf-046bffb47842 | 2024-05-22 | Warnings, Adverse reactions | 65219-028-05 65219-028 65219002805 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.