NDC11 00121065304
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 |
|---|---|
| 00121-0653-04 | 00121-0653 |
| 00121-0653-4 | 00121-0653 |
| 00121-653-04 | 00121-653 |
| 0121-0653-04 | 0121-0653 |
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 |
|---|---|---|---|---|---|---|
| Fluphenazine Hydrochloride | FLUPHENAZINE HYDROCHLORIDE | PAI Holdings, LLC dba PAI Pharma | 0860b3f3-3116-40f8-bcb0-e5c47731bdc8 | 2025-01-23 | Boxed warning, Warnings, Adverse reactions | 0121-0653-04 0121-0653 00121065304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.