NDC11 65219029002
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 |
|---|---|
| 65219-0290-02 | 65219-0290 |
| 65219-0290-2 | 65219-0290 |
| 65219-290-02 | 65219-290 |
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 |
|---|---|---|---|---|---|---|
| cetrorelix acetate | CETRORELIX ACETATE | FRESENIUS KABI USA, LLC | c9c50fcb-b28d-4085-9116-b38a21d31b99 | 2024-07-12 | Warnings, Adverse reactions | 65219-290-02 65219029002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.