NDC11 00220159841

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
00220-1598-41	00220-1598
0220-1598-41	0220-1598

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
CUPRUM ARSENICOSUM	CUPRIC ARSENITE	Boiron	3b3d374a-78cb-f2eb-e063-6294a90a0f29	2025-07-31		Exact identifier ndc (package): 0220-1598-41 ndc (product): 0220-1598 ndc11 (package): 00220159841

Reported adverse events (FAERS/openFDA)#

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