NDC11 71205023102
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 |
|---|---|
| 71205-0231-02 | 71205-0231 |
| 71205-0231-2 | 71205-0231 |
| 71205-231-02 | 71205-231 |
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 |
|---|---|---|---|---|---|---|
| Sildenafil Citrate | SILDENAFIL | Proficient Rx LP | 3522bdcc-8113-4562-8ca1-f3eb884beaea | 2026-06-01 | Warnings, Adverse reactions | 71205-231-02 71205-231 71205023102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.