NDC11 00069024230

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
00069-0242-3000069-0242
00069-242-3000069-242
0069-0242-300069-0242

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
ToviazFESOTERODINE FUMARATEPfizer Laboratories Div Pfizer Inc5be745f0-8ae7-4c3c-9962-37d6263326f12026-04-07Warnings, Adverse reactionsExact identifier
ndc (package): 0069-0242-30
ndc (product): 0069-0242
ndc11 (package): 00069024230

Reported adverse events (FAERS/openFDA)#

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