NDC11 70069023101
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 |
|---|---|
| 70069-0231-01 | 70069-0231 |
| 70069-0231-1 | 70069-0231 |
| 70069-231-01 | 70069-231 |
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 |
|---|---|---|---|---|---|---|
| BRIMONIDINE TARTRATE | BRIMONIDINE TARTRATE | Somerset Therapeutics, LLC | cdb8620f-adfa-4433-b285-9c42334f8600 | 2025-03-22 | Warnings, Adverse reactions | 70069-231-01 70069-231 70069023101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.