NDC11 00009001305
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 |
|---|---|
| 00009-0013-05 | 00009-0013 |
| 00009-0013-5 | 00009-0013 |
| 00009-013-05 | 00009-013 |
| 0009-0013-05 | 0009-0013 |
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 |
|---|---|---|---|---|---|---|
| Solu-Cortef | HYDROCORTISONE SODIUM SUCCINATE | Pharmacia & Upjohn Company LLC | 65eefd58-b166-4d71-ade6-45c8fdf86922 | 2026-08-27 | Warnings, Adverse reactions | 0009-0013-05 0009-0013 00009001305 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.