Topiramate

Product NDC

68788-8967

11-digit product format

687888967

Labeler code

68788

Product ID

68788-8967_a6ce422a-bc71-49da-a916-b1b747a2fbb4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Topiramate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals

Application

ANDA077627

Marketing category

ANDA

Marketing start

2016-01-11

Marketing end

0000-00-00

Substance

TOPIRAMATE

Active strength

100 mg/1

Pharmacologic classes

Decreased Centr

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record