NDC11 43975032309
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 |
|---|---|
| 43975-0323-09 | 43975-0323 |
| 43975-0323-9 | 43975-0323 |
| 43975-323-09 | 43975-323 |
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 |
|---|---|---|---|---|---|---|
| Tolterodine Tartrate | TOLTERODINE TARTRATE | ANI Pharmaceuticals, Inc. | fc5bdc4a-a483-4d31-807b-c7f8d8869723 | 2025-04-01 | Warnings, Adverse reactions | 43975-323-09 43975-323 43975032309 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.