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FDA ANDA · ANDA040187

THIORIDAZINE HYDROCHLORIDE

Sponsor: PHARM ASSOC

APPLICATION
ANDA040187
TYPE
ANDA
ORIGINAL APPROVAL
1997-08-28
LATEST ACTION
2025-01-22
ROUTE
ORAL
DOSAGE FORM
CONCENTRATE
MARKETING STATUS
Discontinued

Products

THIORIDAZINE HYDROCHLORIDEDiscontinued
THIORIDAZINE HYDROCHLORIDE 30MG/ML · CONCENTRATE · ORAL

Approval history

2025-01-22Labeling · Supplement 5 · standardAP
2017-02-23Labeling · Supplement 4 · standardAP
2010-12-06Labeling · Supplement 3AP
2002-10-31Labeling · Supplement 1AP
1997-08-28OriginalReviewAP
VIEW ON DRUGS@FDA ↗

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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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