NDC11 69489020130
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 |
|---|---|
| 69489-0201-30 | 69489-0201 |
| 69489-201-30 | 69489-201 |
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 |
|---|---|---|---|---|---|---|
| AMZEEQ | MINOCYCLINE | Journey Medical Corporation | cc251492-977b-4eb1-a088-a90831324bad | 2023-10-01 | Warnings, Adverse reactions | 69489-201-30 69489-201 69489020130 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.