NDC11 71205009660
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 |
|---|---|
| 71205-0096-60 | 71205-0096 |
| 71205-096-60 | 71205-096 |
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 |
|---|---|---|---|---|---|---|
| Atenolol | ATENOLOL | Proficient Rx LP | c3a23869-1e3f-40f0-9726-833700580113 | 2019-10-01 | Boxed warning, Warnings, Adverse reactions | 71205-096-60 71205-096 71205009660 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.