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FDA ANDA · ANDA077555

TIAGABINE HYDROCHLORIDE

Sponsor: SUN PHARM INDS

APPLICATION
ANDA077555
TYPE
ANDA
ORIGINAL APPROVAL
2011-11-04
LATEST ACTION
2011-11-04
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

TIAGABINE HYDROCHLORIDEDiscontinued
TIAGABINE HYDROCHLORIDE 4MG · TABLET · ORAL
TIAGABINE HYDROCHLORIDEDiscontinued
TIAGABINE HYDROCHLORIDE 2MG · TABLET · ORAL

Approval history

2011-11-04Original — Letter ↗AP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industry →GMP discipline →FDA drug shortages →FDA enforcement & recalls →

Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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