NDC11 00615823705

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
00615-8237-05	00615-8237
00615-8237-5	00615-8237
0615-8237-05	0615-8237

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	NCS HealthCare of KY, LLC dba Vangard Labs	388fd4bc-f12f-4e55-a1e7-72aa585519fa	2024-09-17	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0615-8237-05 ndc (product): 0615-8237 ndc11 (package): 00615823705

Reported adverse events (FAERS/openFDA)#

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