NDC11 62332082131

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 NDC	Product root
62332-0821-31	62332-0821
62332-821-31	62332-821

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Divalproex sodium	DIVALPROEX SODIUM	Alembic Pharmaceuticals Inc.	fea19b14-d8ed-4954-bc54-b9240f78b3c3	2026-04-08	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 62332-821-31 ndc (product): 62332-821 ndc11 (package): 62332082131

Reported adverse events (FAERS/openFDA)#

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