NDC11 63323031510
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 |
|---|---|
| 63323-0315-10 | 63323-0315 |
| 63323-315-10 | 63323-315 |
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 |
|---|---|---|---|---|---|---|
| Ganciclovir | GANCICLOVIR SODIUM | Fresenius Kabi USA, LLC | b47f5d1c-36b8-49b6-a410-3b3f4661dde7 | 2026-01-09 | Boxed warning, Warnings, Adverse reactions | 63323-315-10 63323-315 63323031510 |
| Ganciclovir | GANCICLOVIR SODIUM | Fresenius Kabi USA, LLC | 35addab5-09db-4f8a-9c69-6fbce33ecc37 | 2026-01-09 | Boxed warning, Warnings, Adverse reactions | 63323-315 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.