NDC11 00121107601
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 |
|---|---|
| 00121-1076-01 | 00121-1076 |
| 00121-1076-1 | 00121-1076 |
| 0121-1076-01 | 0121-1076 |
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 |
|---|---|---|---|---|---|---|
| Mupirocin | MUPIROCIN | PAI Holdings, LLC dba PAI Pharma | a822d44d-c651-406c-a2b9-aa8fbe8f89ce | 2026-03-17 | Warnings, Adverse reactions | 0121-1076-01 0121-1076 00121107601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.