NDC11 63479060701
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 |
|---|---|
| 63479-0607-01 | 63479-0607 |
| 63479-0607-1 | 63479-0607 |
| 63479-607-01 | 63479-607 |
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 |
|---|---|---|---|---|---|---|
| F07 LVJY | ALOE VERA, BIG SAGEBRUSH, BORAGE, CALIFORNIA WILDROSE, CALOCHORTUS GUNNISONII, CAUSTICUM, CHICORY, COFFEA CRUDA, CROCUS SATIVUS, DICENTRA FORMOSA, DIPLACUS AURANTIACUS, ENGLISH HAWTHRON, ENGLISH HOLLY, EUROPEAN ASPEN, FLOWERING QUINCE, FORKING LARKSPUR, MIMULUS GUTTATUS, NASTURTIUM, PHOSPHORICUM ACIDUM, STROPHANTHUS HISPIDUS, WILD MUSTARD, YELLOW STAR THISTLE, YERBA SANTA, ZINNIA ELEGANS | Apex Energetics Inc. | bc928980-0f46-7e49-e053-2995a90a2253 | 2024-01-08 | Warnings | 63479-0607-1 63479-0607 63479060701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.