NDC11 77617002302
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 |
|---|---|
| 77617-0023-02 | 77617-0023 |
| 77617-0023-2 | 77617-0023 |
| 77617-023-02 | 77617-023 |
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 |
|---|---|---|---|---|---|---|
| Metro Antimicrobial Hand | BENZALKONIUM CHLORIDE | Maintex | a84d83dd-2445-4d0f-b763-2c69e8248cf9 | 2025-11-06 | Warnings | 77617-023-02 77617-023 77617002302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.