Divalproex Sodium

Product NDC

0615-7531

11-digit product format

006157531

Labeler code

0615

Product ID

0615-7531_1fbb3a5a-960b-45f5-8fe2-2cea7685617a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Divalproex Sodium

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA078182

Marketing category

ANDA

Marketing start

2011-01-21

Marketing end

0000-00-00

Substance

DIVALPROEX SODIUM

Active strength

125 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record