Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 088737
Company: SUN PHARM INDUSTRIES
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
THIORIDAZINE HYDROCHLORIDE THIORIDAZINE HYDROCHLORIDE 150MG TABLET;ORAL Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
09/26/1984 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
02/23/2017 SUPPL-22 Labeling-Package Insert

Label is not available on this site.

12/03/2010 SUPPL-21 Labeling-Package Insert

Label is not available on this site.

12/01/1998 SUPPL-20 Manufacturing (CMC)

Label is not available on this site.

12/23/1994 SUPPL-19 Manufacturing (CMC)

Label is not available on this site.

10/11/1994 SUPPL-18 Manufacturing (CMC)

Label is not available on this site.

04/03/1992 SUPPL-17 Manufacturing (CMC)

Label is not available on this site.

04/03/1992 SUPPL-15 Manufacturing (CMC)

Label is not available on this site.

02/23/1990 SUPPL-13 Labeling

Label is not available on this site.

07/08/1991 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

08/19/1988 SUPPL-10 Labeling

Label is not available on this site.

06/02/1988 SUPPL-9 Labeling

Label is not available on this site.

03/03/1988 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

04/01/1987 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

02/14/1986 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

02/14/1986 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

04/23/1985 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

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