NDC11 65862080210
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 |
|---|---|
| 65862-0802-10 | 65862-0802 |
| 65862-802-10 | 65862-802 |
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 |
|---|---|---|---|---|---|---|
| Bimatoprost | BIMATOPROST | Aurobindo Pharma Limited | 059a60ec-aee2-4c13-8307-05cd92e8729a | 2023-07-17 | Warnings, Adverse reactions | 65862-802-10 65862-802 65862080210 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.