NDC11 00078142015

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
00078-1420-1500078-1420
0078-1420-150078-1420

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
VANRAFIAATRASENTANNovartis Pharmaceuticals Corporation9a7e7f85-bfd0-44a0-beda-3bcfa8215c642026-06-12Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 0078-1420-15
ndc (product): 0078-1420
ndc11 (package): 00078142015

Reported adverse events (FAERS/openFDA)#

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