Divalproex Sodium

Manufacturer: Hahnenmann Laboratories, Inc. | Hahnemann Laboratories, Inc.
Effective date: 2017-05-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:08:42

Label at a glance#

ProductDivalproex Sodium

Active ingredientDIVALPROEX SODIUM

Label structure1 sections

Label contents#

Full prescribing information#

Single label image contains content for sections 1-17.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

img

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
b10a892b-b985-4cbc-9547-9ac4b72b784f	Product name	2	20250818
7a3a03f1-382a-f9ec-0741-ff24dcbfed69	Product name	7	20250624
57fc3d01-4737-4091-9728-9e8a4c9e708d	Product name	1	20200121
5d67ecc7-47c7-ec5e-e9eb-71bf00250645	Product name	1	20140508
97fce1a8-50c4-f088-0e31-64d82b6e9081	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63545-678-01	2020-01-31	C162847	48780-1	9d75b9d0-d9a2-f424-e053-dadaa90a57ce	4eb51bae-ae01-52e3-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63545-678-01	Divalproex Sodium	240 [hp_C] in 1 VIAL, GLASS	PELLET	240		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63545-678	DIVALPROEX SODIUM PELLET [HAHNENMANN LABORATORIES, INC.]	1	Legacy NDC, 1 package rows	20170510_4eb51bae-ae01-52e3-e054-00144ff8d46c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Divalproex Sodium
VALPROIC ACID
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63545-678	63545-678-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIVALPROEX SODIUM	644VL95AO6	ACTIM
SUCROSE	C151H8M554	IACT

Source Document#

Source XML

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
4eb51bae-ae02-52e3-e054-00144ff8d46c			4eb51bae-ae01-52e3-e054-00144ff8d46c	2017-05-04		Exact identifier spl id: 4eb51bae-ae02-52e3-e054-00144ff8d46c spl set id: 4eb51bae-ae01-52e3-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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