NDC11 71205029490
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 |
|---|---|
| 71205-0294-90 | 71205-0294 |
| 71205-294-90 | 71205-294 |
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 |
|---|---|---|---|---|---|---|
| Pravastatin Sodium | PRAVASTATIN SODIUM | Proficient Rx LP | 466e2d1a-a6d6-40f8-a9f6-3e7494a34ca6 | 2023-08-01 | Warnings, Adverse reactions | 71205-294-90 71205-294 71205029490 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.