Divalproex Sodium

Product NDC

50090-3156

11-digit product format

500903156

Labeler code

50090

Product ID

50090-3156_eb052cd5-8bab-4d18-9e5c-e008e7934968

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Divalproex Sodium

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA090161

Marketing category

ANDA

Marketing start

2013-08-11

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record