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FDA ANDA · ANDA088564

THIORIDAZINE HYDROCHLORIDE

Sponsor: WATSON LABS

APPLICATION
ANDA088564
TYPE
ANDA
ORIGINAL APPROVAL
1984-05-11
LATEST ACTION
2017-02-24
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

THIORIDAZINE HYDROCHLORIDEDiscontinued
THIORIDAZINE HYDROCHLORIDE 100MG · TABLET · ORAL

Approval history

2017-02-24Labeling · Supplement 26 · standardAP
2015-11-03Labeling · Supplement 25AP
1997-01-31Manufacturing (CMC) · Supplement 23AP
1991-02-04Labeling · Supplement 22AP
1990-09-17Labeling · Supplement 24AP
1988-07-05Labeling · Supplement 20AP
1988-07-05Labeling · Supplement 21AP
1988-06-09Manufacturing (CMC) · Supplement 18AP
1988-06-09Manufacturing (CMC) · Supplement 17AP
1988-04-22Labeling · Supplement 19AP
1987-11-06Manufacturing (CMC) · Supplement 16AP
1987-05-15Manufacturing (CMC) · Supplement 14AP
1985-11-26Manufacturing (CMC) · Supplement 7AP
1985-11-26Manufacturing (CMC) · Supplement 10AP
1985-11-26Manufacturing (CMC) · Supplement 8AP
1985-10-08Manufacturing (CMC) · Supplement 5AP
1985-10-08Manufacturing (CMC) · Supplement 4AP
1984-05-11OriginalAP
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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