NDC11 00220023041

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
00220-0230-41	00220-0230
00220-230-41	00220-230
0220-0230-41	0220-0230

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
AMBROSIA ARTEMISIAEFOLIA	AMBROSIA ARTEMISIIFOLIA	Boiron	0c069179-fc7c-cf6b-e063-6394a90aeaeb	2023-12-08		Exact identifier ndc (package): 0220-0230-41 ndc (product): 0220-0230 ndc11 (package): 00220023041

Reported adverse events (FAERS/openFDA)#

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