Drugplain

NDC 0093-5031-56

Tiagabine Hydrochloride 4 mg/1

Tiagabine Hydrochloride · TABLET, FILM COATED

No Recall History

Tiagabine Hydrochloride is a tablet, film coated containing tiagabine hydrochloride at a strength of 4 mg/1. Manufactured by Teva Pharmaceuticals USA, Inc..

Key Facts

Brand Name
Tiagabine Hydrochloride
Generic Name
Tiagabine Hydrochloride
NDC Code (Package)
0093-5031-56
NDC Code (Product)
0093-5031
Manufacturer
Teva Pharmaceuticals USA, Inc.
Strength
4 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
NDA020646
Marketing Start
06/03/2016

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.