NDC11 42543072601
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 |
|---|---|
| 42543-0726-01 | 42543-0726 |
| 42543-0726-1 | 42543-0726 |
| 42543-726-01 | 42543-726 |
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 |
|---|---|---|---|---|---|---|
| Fluoxetine | FLUOXETINE HYDROCHLORIDE | Vensun Pharmaceuticals, Inc. | b4f37ef1-8f5e-4318-90f1-2d8f8afb669c | 2017-09-18 | Boxed warning, Warnings, Adverse reactions | 42543-726-01 42543-726 42543072601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.