NDC11 43857064501

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
43857-0645-01	43857-0645
43857-0645-1	43857-0645
43857-645-01	43857-645

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
Epiforce P	BAPTISIA TINCTORIA, BERBERIS VULGARIS, ECHINACEA (ANGUSTIFOLIA), GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, TRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, ARSENICUM IODATUM, CALCAREA CARBONICA, CLEMATIS ERECTA, GRAPHITES, KALI MURIATICUM, KALI SULPHURICUM, MEZEREUM PETROLEUM, SEPIA	BioActive Nutritional, Inc.	d33282bf-2045-4b92-a377-013fa711c877	2024-12-12	Warnings	Exact identifier ndc (package): 43857-0645-1 ndc (product): 43857-0645 ndc11 (package): 43857064501

Reported adverse events (FAERS/openFDA)#

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