Divalproex Sodium

Product NDC

0115-6922

11-digit product format

001156922

Labeler code

0115

Product ID

0115-6922_09f86269-2e96-4566-8618-b73baf128bcc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DIVALPROEX SODIUM

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Impax Generics

Application

ANDA078791

Marketing category

ANDA

Marketing start

2009-08-04

Marketing end

2019-10-31

Substance

DIVALPROEX SODIUM

Active strength

500 mg/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

0000-00-00

Current FDA listing

Historical FDA.report record