NDC11 44911058101
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 |
|---|---|
| 44911-0581-01 | 44911-0581 |
| 44911-0581-1 | 44911-0581 |
| 44911-581-01 | 44911-581 |
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 |
|---|---|---|---|---|---|---|
| Histapoll HP | ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, APIS MELLFICA, ARSENICUM ALBUM, EUPHRASIA OFFICINALIS, NUX VOMICA, PHOSPHORUS, PULSATILLA (VULGARIS), SOLIDAGO VIRGAUREA, SULPHUR | Energique, Inc. | 09a75182-6939-4e2b-a61a-9c58c9e9284e | 2023-04-21 | Warnings | 44911-0581-1 44911-0581 44911058101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.