NDC11 59469014050
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 |
|---|---|
| 59469-0140-50 | 59469-0140 |
| 59469-140-50 | 59469-140 |
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 |
|---|---|---|---|---|---|---|
| MUNDIPUR | BRYONIA DIOICA ROOT, COLCHICUM AUTUMNALE BULB, SODIUM CARBONATE, PHYTOLACCA AMERICANA ROOT, BERBERIS VULGARIS ROOT BARK, CYNARA SCOLYMUS WHOLE, HARPAGOPHYTUM PROCUMBENS ROOT, AND LEDUM PALUSTRE TWIG | PEKANA Naturheilmittel GmbH | 4aeba0c8-0d53-4012-8024-df1e82585cb3 | 2022-12-16 | Warnings | 59469-140-50 59469-140 59469014050 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.