NDC11 63323082301
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 |
|---|---|
| 63323-0823-01 | 63323-0823 |
| 63323-0823-1 | 63323-0823 |
| 63323-823-01 | 63323-823 |
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 |
|---|---|---|---|---|---|---|
| Ertapenem | ERTAPENEM SODIUM | Fresenius Kabi USA, LLC | 666c9f33-ea9e-4667-b8bd-f8b1b6b6be51 | 2022-11-08 | Warnings, Adverse reactions | 63323-823-01 63323-823 63323082301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.