NDC11 44911068501
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 |
|---|---|
| 44911-0685-01 | 44911-0685 |
| 44911-0685-1 | 44911-0685 |
| 44911-685-01 | 44911-685 |
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 |
|---|---|---|---|---|---|---|
| Anxiety | ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, CARCINOSIN, CAUSTICUM, GELSEMIUM SEMPERVIRENS, LACHESIS MUTUS, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, MERCURIUS VIVUS, NITRICUM ACIDUM, PHOSPHORUS, RHUS TOX | Energique, Inc. | 2fd7051b-d274-4028-8348-b175a22f045c | 2023-11-03 | Warnings | 44911-0685-1 44911-0685 44911068501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.