NDC11 50845009201

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
50845-0092-01	50845-0092
50845-0092-1	50845-0092
50845-092-01	50845-092

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
Menopause	AGNUS CASTUS, ANGELICA SINENSIS RADIX, APIS MELLIFICA, ARALIA QUINQUEFOLIA, ARNICA MONTANA, CIMICIFUGA RACEMOSA, GALIUM APARINE, GLYCYRRHIZA GLABRA, OOPHORINUM SUIS, SEPIA, THUJA OCCIDENTALIS, VISCUM ALBUM	Liddell Laboratories, Inc.	3e17fa78-f5c2-47eb-9bb6-075ccffd01b6	2024-07-01	Warnings	Exact identifier ndc (package): 50845-0092-1 ndc (product): 50845-0092 ndc11 (package): 50845009201

Reported adverse events (FAERS/openFDA)#

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