NDC11 00121088508
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 |
|---|---|
| 00121-0885-08 | 00121-0885 |
| 00121-0885-8 | 00121-0885 |
| 00121-885-08 | 00121-885 |
| 0121-0885-08 | 0121-0885 |
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 |
|---|---|---|---|---|---|---|
| Prednisolone | PREDNISOLONE | PAI Holdings, LLC dba PAI Pharma | cebd7b5b-8e9f-4de9-9fcf-8ee0661fede3 | 2024-08-19 | Warnings, Adverse reactions | 0121-0885-08 0121-0885 00121088508 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.