Divalproex Sodium

Product NDC

0615-7849

11-digit product format

006157849

Labeler code

0615

Product ID

0615-7849_a02d04f2-7ff7-43cc-b949-17a055c6861e

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

ANDA077100

Marketing category

ANDA

Marketing start

2010-03-06

Marketing end

0000-00-00

Substance

DIVALPROEX SODIUM

Active strength

250 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