NDC11 71205072830
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 |
|---|---|
| 71205-0728-30 | 71205-0728 |
| 71205-728-30 | 71205-728 |
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 |
|---|---|---|---|---|---|---|
| Levetiracetam ER | LEVETIRACETAM | Proficient Rx LP | a0ad8200-70c9-4f4f-86c5-4a8c6c9f0223 | 2022-12-01 | Warnings, Adverse reactions | 71205-728-30 71205-728 71205072830 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.