NDC11 71335273707
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 |
|---|---|
| 71335-2737-07 | 71335-2737 |
| 71335-2737-7 | 71335-2737 |
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 |
|---|---|---|---|---|---|---|
| PredniSONE Tablets, USP, 20 mg | PREDNISONE | Bryant Ranch Prepack | bfcc98b8-184e-4db4-8079-de88958c774b | 2025-09-26 | Warnings, Adverse reactions | 71335-2737-7 71335-2737 71335273707 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.