NDC11 44911058701

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 table
Package NDC	Product root
44911-0587-01	44911-0587
44911-0587-1	44911-0587
44911-587-01	44911-587

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Joint Tone AI	CIMICIFUGA RACEMOSA, LAPPA MAJOR, TRIFOLIUM PRATENSE, COLCHICUM AUTUMNALE, DULCAMARA, LYCOPODIUM CLAVATUM, PULSATILLA (PRATENSIS), RHODODENDRON CHRYSANTHUM, RHUS TOX	Energique, Inc.	bcd543aa-eb43-455e-9a73-37323f050e24	2023-10-04	Warnings	Exact identifier ndc (package): 44911-0587-1 ndc (product): 44911-0587 ndc11 (package): 44911058701

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.