FDA.reportPublic FDA data

NDC11 31722002201

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
31722-0022-0131722-0022
31722-0022-131722-0022
31722-022-0131722-022

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
Divalproex sodiumDIVALPROEX SODIUMCamber Pharmaceuticals, Inc.e8e954d4-54e3-491c-867c-b3b656b70f232026-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 31722-022-01
ndc (product): 31722-022
ndc11 (package): 31722002201

Reported adverse events (FAERS/openFDA)#

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