NDC11 00121088508

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
00121-0885-0800121-0885
00121-0885-800121-0885
00121-885-0800121-885
0121-0885-080121-0885

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
PrednisolonePREDNISOLONEPAI Holdings, LLC dba PAI Pharmacebd7b5b-8e9f-4de9-9fcf-8ee0661fede32024-08-19Warnings, Adverse reactionsExact identifier
ndc (package): 0121-0885-08
ndc (product): 0121-0885
ndc11 (package): 00121088508

Reported adverse events (FAERS/openFDA)#

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