NDC11 00009379401

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
00009-3794-0100009-3794
00009-3794-100009-3794
0009-3794-010009-3794

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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CorvertIBUTILIDE FUMARATEPharmacia & Upjohn Company LLC2428969a-7431-4e94-9503-ad5c680e2ea42024-01-25Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (product): 0009-3794
CorvertIBUTILIDE FUMARATEPharmacia & Upjohn Company LLCb7d717ed-022d-4459-b5e6-098c2a8b74272024-01-25Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 0009-3794-01
ndc (product): 0009-3794
ndc11 (package): 00009379401

Reported adverse events (FAERS/openFDA)#

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