NDC11 65862016801
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 |
|---|---|
| 65862-0168-01 | 65862-0168 |
| 65862-0168-1 | 65862-0168 |
| 65862-168-01 | 65862-168 |
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 | Aurobindo Pharma Limited | 1b8a4689-3916-4f4b-b54a-bbb4e322d79b | 2024-02-21 | Warnings, Adverse reactions | 65862-168-01 65862-168 65862016801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.