TOPIRAMATE

Product NDC

68788-9730

11-digit product format

687889730

Labeler code

68788

Product ID

68788-9730_8c1cfa0d-1c88-4e97-af52-7d5cd989276f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

topiramate

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals

Application

ANDA079153

Marketing category

ANDA

Marketing start

2012-10-31

Marketing end

0000-00-00

Substance

TOPIRAMATE

Active strength

25 mg/1

Pharmacologic classes

Decreased Centr

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record