NDC11 59469031110
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 |
|---|---|
| 59469-0311-10 | 59469-0311 |
| 59469-311-10 | 59469-311 |
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 |
|---|---|---|---|---|---|---|
| KLIFEM | ALETRIS FARINOSA ROOT, GRAPHITE, CHAMAELIRIUM LUTEUM ROOT, PILOCARPUS JABORANDII LEAF, LACHESIS MUTA VENOM, ANEMONE PRATENSIS FLOWERING TOP, SANGUINARIA CANADENSIS ROOT, AND LAMIUM ALBUM FLOWERING TOP | PEKANA Naturheilmittel GmbH | 6193b54f-cb07-43da-a18e-18c123e9179b | 2023-01-11 | Warnings | 59469-311-10 59469-311 59469031110 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.