NDC11 44911025801
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 |
|---|---|
| 44911-0258-01 | 44911-0258 |
| 44911-0258-1 | 44911-0258 |
| 44911-258-01 | 44911-258 |
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 |
|---|---|---|---|---|---|---|
| Menotone | ANGELICA ARCHANGELICA, CIMICIFUGA RACEMOSA, BELLADONNA, LACHESIS MUTUS, PULSATILLA (PRATENSIS), SABINA, SANGUINARIA CANADENSIS, SEPIA, SULPHUR | Energique, Inc. | 0921be57-44b4-4d1c-a50a-7886fc807d00 | 2024-01-23 | Warnings | 44911-0258-1 44911-0258 44911025801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.