Topiramate

Product NDC

68788-6366

11-digit product format

687886366

Labeler code

68788

Product ID

68788-6366_1f09784a-252c-441b-8366-391fab791ac8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Topiramate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticalc

Application

ANDA077627

Marketing category

ANDA

Marketing start

2009-03-27

Marketing end

0000-00-00

Substance

TOPIRAMATE

Active strength

50 mg/1

Pharmacologic classes

Decreased Centr

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record