Divalproex Sodium

Product NDC: 37662-0732
11-digit product format: 376620732
Labeler code: 37662
Product ID: 37662-0732_e3281609-460b-4982-e053-2995a90a01c5
Type: HUMAN OTC DRUG
Nonproprietary name: Divalproex Sodium
Dosage form: PELLET
Route: ORAL
Labeler: Hahnemann Laboratories, INC.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2022-07-06
Substance: VALPROATE SODIUM
Active strength: 1 [hp_Q]/1
Pharmacologic classes: Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Divalproex Sodium
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
VALPROATE SODIUM	1 [hp_Q]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5VOM6GYJ0D	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
e3281609-460a-4982-e053-2995a90a01c5	Available on FDA.report

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
37662-0732-1	Divalproex Sodium	10000 in 1 BOTTLE, GLASS	PELLET	10000		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37662-0732	DIVALPROEX SODIUM PELLET [HAHNEMANN LABORATORIES, INC.]	1	Current NDC, Legacy NDC, 1 package rows	20221223_e3281609-460a-4982-e053-2995a90a01c5.zip

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	Hahnemann Laboratories, INC.	e3281609-460a-4982-e053-2995a90a01c5	2022-07-06		Exact identifier ndc (product): 37662-0732

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5VOM6GYJ0D	VALPROATE SODIUM	1069-66-5	VALPROATE SODIUM
644VL95AO6	DIVALPROEX SODIUM	76584-70-8	Divalproex Sodium

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
37662-0732-1	37662073201	10000 PELLET in 1 BOTTLE, GLASS (37662-0732-1)	10000 pellet	2022-07-06	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Divalproex Sodium - Hahnemann Laboratories, INC.	Hahnemann Laboratories, INC.	2022-07-06	HUMAN OTC DRUG LABEL	1