NDC 72205-085

Tiagabine Hydrochloride 4 mg tablet

On the label: Novadoz Pharmaceuticals LLC.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
MSN Laboratories Private LimitedRangareddy District, IndiaMakes it and tests it Problems found, fixed voluntarilyDec 21, 2023 · 4 inspections

Product details

Generic drug
Tiagabine: every company that makes it
Form
tablet, oral
Strength
4 mg
Approval
ANDA ANDA214816
On the market since
Nov 23, 2021
Package NDCs
72205-085-30
Official label
DailyMed (National Library of Medicine), updated Mar 1, 2021

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