NDC11 59208000130
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 |
|---|---|
| 59208-0001-30 | 59208-0001 |
| 59208-001-30 | 59208-001 |
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 |
|---|---|---|---|---|---|---|
| Conazol | MICONAZOLE NITRATE | Laboratorios Liomont, S.A. de C.V. | 84780538-8618-5750-e053-2a91aa0a6054 | 2025-07-07 | Warnings | 59208-001-30 59208-001 59208000130 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.