NDC11 71921040010
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 |
|---|---|
| 71921-0400-10 | 71921-0400 |
| 71921-400-10 | 71921-400 |
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 |
|---|---|---|---|---|---|---|
| Dorzolamide Hydrochloride Ophthalmic | DORZOLAMIDE HYDROCHLORIDE OPHTHALMIC | Florida Pharmaceutical Products, LLC | e4e6a5a8-f7be-4424-83f2-d6bb4d57443e | 2026-06-24 | Warnings, Adverse reactions | 71921-400-10 71921-400 71921040010 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.