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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 087862
Company: SUN PHARM INDUSTRIES
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
HYDROXYZINE HYDROCHLORIDE HYDROXYZINE HYDROCHLORIDE 100MG 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
04/18/1983 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
11/08/2016 SUPPL-17 Labeling-Package Insert

Label is not available on this site.

03/30/2016 SUPPL-16 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

06/03/2014 SUPPL-15 Labeling-Package Insert

Label is not available on this site.

12/01/1998 SUPPL-14 Manufacturing (CMC)

Label is not available on this site.

12/23/1994 SUPPL-13 Manufacturing (CMC)

Label is not available on this site.

10/11/1994 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

04/03/1992 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

04/03/1992 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

12/08/1987 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

04/01/1987 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

11/20/1984 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

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