NDC11 63323062100
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 |
|---|---|
| 63323-0621-0 | 63323-0621 |
| 63323-0621-00 | 63323-0621 |
| 63323-621-00 | 63323-621 |
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 |
|---|---|---|---|---|---|---|
| Pemetrexed | PEMETREXED DISODIUM | Fresenius Kabi USA, LLC | ae77f00f-d43b-4b75-afd5-a2a9cb7138da | 2025-08-31 | Warnings, Adverse reactions | 63323-621-00 63323-621 63323062100 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.