NDC11 00121094205
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 |
|---|---|
| 00121-0942-05 | 00121-0942 |
| 00121-0942-5 | 00121-0942 |
| 00121-942-05 | 00121-942 |
| 0121-0942-05 | 0121-0942 |
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 |
|---|---|---|---|---|---|---|
| Phenobarbital Oral Solution | PHENOBARBITAL ORAL | PAI Holdings, LLC dba PAI Pharma | 30c20889-2b12-4d73-b4ce-0e1b49b3e3c3 | 2024-11-19 | Warnings, Adverse reactions | 0121-0942-05 0121-0942 00121094205 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.