NDC11 00143956801

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
00143-9568-0100143-9568
00143-9568-100143-9568
0143-9568-010143-9568

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
CefuroximeCEFUROXIMEHikma Pharmaceuticals USA Inc.19902965-d2d6-433f-982d-0095014df4e82018-09-27Warnings, Adverse reactionsExact identifier
ndc (package): 0143-9568-01
ndc (product): 0143-9568
ndc11 (package): 00143956801

Reported adverse events (FAERS/openFDA)#

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