NDC11 63323019202
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 |
|---|---|
| 63323-0192-02 | 63323-0192 |
| 63323-0192-2 | 63323-0192 |
| 63323-192-02 | 63323-192 |
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 |
|---|---|---|---|---|---|---|
| Fludarabine | FLUDARABINE PHOSPHATE | Fresenius Kabi USA, LLC | cf5255cc-91fd-4132-973b-764dba142eae | 2024-10-14 | Boxed warning, Warnings, Adverse reactions | 63323-192-02 63323-192 63323019202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.