tiagabine hydrochloride

Product NDC

52536-350

11-digit product format

525360350

Labeler code

52536

Product ID

52536-350_60ed80ce-3279-41a6-8bdc-7c8545ceaab0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

tiagabine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Wilshire Pharmaceuticals, Inc.

Application

ANDA206857

Marketing category

ANDA

Marketing start

2018-06-01

Marketing end

0000-00-00

Substance

TIAGABINE HYDROCHLORIDE

Active strength

2 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record