NDC11 59651071246

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
59651-0712-4659651-0712
59651-712-4659651-712

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
TretinoinTRETINOINAurobindo Pharma Limitedf64e45d7-bbc0-4da4-9ccb-e3941f22fdbe2025-06-18Warnings, Adverse reactionsExact identifier
ndc (package): 59651-712-46
ndc (product): 59651-712
ndc11 (package): 59651071246

Reported adverse events (FAERS/openFDA)#

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