NDC11 23155003005
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 |
|---|---|
| 23155-0030-05 | 23155-0030 |
| 23155-0030-5 | 23155-0030 |
| 23155-030-05 | 23155-030 |
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 | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 6f4e4e9f-9ded-452f-b3ef-ab6aa9c72952 | 2026-08-11 | Boxed warning, Warnings, Adverse reactions | 23155-030-05 23155-030 23155003005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.