NDC11 21130010502
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 |
|---|---|
| 21130-0105-02 | 21130-0105 |
| 21130-0105-2 | 21130-0105 |
| 21130-105-02 | 21130-105 |
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 |
|---|---|---|---|---|---|---|
| Olopatadine Hydrochloride Ophthalmic Solution | OLOPATADINE HYDROCHLORIDE OPHTHALMIC | Albertsons Companies | 685192af-d729-3066-5825-6d0e03ce787e | 2025-12-12 | Warnings | 21130-105-02 21130-105 21130010502 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.