NDC11 63323096600
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 |
|---|---|
| 63323-0966-0 | 63323-0966 |
| 63323-0966-00 | 63323-0966 |
| 63323-966-00 | 63323-966 |
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 |
|---|---|---|---|---|---|---|
| Zoledronic Acid | ZOLEDRONIC ACID | Fresenius Kabi USA, LLC | 16fcf8c9-ef8a-4e93-9ee6-acfadd35a861 | 2023-09-21 | Warnings, Adverse reactions | 63323-966-00 63323-966 63323096600 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.