NDC11 44911074401
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 |
|---|---|
| 44911-0744-01 | 44911-0744 |
| 44911-0744-1 | 44911-0744 |
| 44911-744-01 | 44911-744 |
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 |
|---|---|---|---|---|---|---|
| Tree Antigens | ARSENICUM ALBUM, LYCOPODIUM CLAVATUM, PULSATILLA (PRATENSIS), BLACK WILLOW, POLLEN (SALIX NIGRA), BOX ELDER, POLLEN (ACER NEGUNDO), EASTERN COTTONWOOD, POLLEN (POPULUS DELTOIDES), EASTERN WHITE PINE, POLLEN (PINUS STROBUS), PRIVET, POLLEN (LIGUSTRUM VULGARE), RED MAPLE, POLLEN (ACER RUBRUM), RED OAK, POLLEN (QUERCUS RUBRA), RIVER BIRCH, POLLEN (BETULA NIGRA), SWEET GUM, POLLEN (LIQUIDAMBAR STYRACIFLUA), WHITE ASH, POLLEN (FRAXINUS AMERICANA), WHITE MULBERRY, POLLEN (MORUS ALBA) | Energique, Inc. | ca4d0cb8-d283-4d82-9930-2b6b264a8598 | 2026-01-06 | Warnings | 44911-0744-1 44911-0744 44911074401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.