NDC11 44911074301
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 |
|---|---|
| 44911-0743-01 | 44911-0743 |
| 44911-0743-1 | 44911-0743 |
| 44911-743-01 | 44911-743 |
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 |
|---|---|---|---|---|---|---|
| Jointox BB | BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, PHYTOLACCA DECANDRA, BORRELIA BURGDORFERI NOSODE, BABESIA MICROTI, EHRLICHIA NOSODE (CANINE), HEPATITIS B NOSODE, MENINGOCOCCUS NOSODE, ACONITUM NAPELLUS, ARSENICUM ALBUM, BRYONIA (ALBA), CHELIDONIUM MAJUS, COLCHICUM AUTUMNALE, KALMIA LATIFOLIA, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, MERCURIUS VIVUS, PHOSPHORUS, RHUS TOX | Energique, Inc. | 2f8f13cc-5c16-4ce4-952f-43df61fda8c9 | 2026-01-05 | Warnings | 44911-0743-1 44911-0743 44911074301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.