Search by Drug Name or NDC

NDC 31722-0021-01 Divalproex sodium 250 mg/1 Details

Divalproex sodium 250 mg/1

Divalproex sodium is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Camber Pharmaceuticals, Inc.. The primary component is DIVALPROEX SODIUM.

MedlinePlus Drug Summary

Valproic acid is used alone or with other medications to treat certain types of seizures. Valproic acid is also used to treat mania (episodes of frenzied, abnormally excited mood) in people with bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal moods). It is also used to prevent migraine headaches but not to relieve headaches that have already begun. Valproic acid is in a class of medications called anticonvulsants. It works by increasing the amount of a certain natural substance in the brain.

Related Packages: 31722-0021-01
Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Valproic Acid

Product Information

NDC	31722-0021
Product ID	31722-021_07e9401d-041e-2f7d-e063-6394a90a1040
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Divalproex sodium
Proprietary Name Suffix	n/a
Non-Proprietary Name	Divalproex sodium
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	250
Active Ingredient Units	mg/1
Substance Name	DIVALPROEX SODIUM
Labeler Name	Camber Pharmaceuticals, Inc.
Pharmaceutical Class	Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA215527
Listing Certified Through	2024-12-31

Package

NDC 31722-0021-01 (31722002101)

Pricing Information	N/A
NDC Package Code	31722-021-01
Billing NDC	31722002101
Package	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-01)
Marketing Start Date	2023-09-26
NDC Exclude Flag	N