FDA.reportPublic FDA data

NDC11 00220085341

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 NDCProduct root
00220-0853-4100220-0853
00220-853-4100220-853
0220-0853-410220-0853

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BERBERIS AQUIFOLIUMBERBERIS AQUIFOLIUM ROOT BARKBoiron3b3c96d0-56f0-2278-e063-6394a90a5c362025-07-31Exact identifier
ndc (package): 0220-0853-41
ndc (product): 0220-0853
ndc11 (package): 00220085341

Reported adverse events (FAERS/openFDA)#

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