NDC11 44911072701

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
44911-0727-01	44911-0727
44911-0727-1	44911-0727
44911-727-01	44911-727

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
Vascular HP	AESCULUS HIPPOCASTANUM, COLLINSONIA CANADENSIS, ECHINACEA (ANGUSTIFOLIA), HAMAMELIS VIRGINIANA, PULSATILLA (PRATENSIS), ARNICA MONTANA, CARBO VEGETABILIS, GRAPHITES, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PAEONIA OFFICINALIS, SEPIA, HYDROFLUORICUM ACIDUM	Energique, Inc.	b69c6bf7-27f5-4711-a6f9-a2f47b51839d	2025-01-29	Warnings	Exact identifier ndc (package): 44911-0727-1 ndc (product): 44911-0727 ndc11 (package): 44911072701

Reported adverse events (FAERS/openFDA)#

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