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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 077820
Company: SUN PHARM INDS INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
GLIPIZIDE GLIPIZIDE 5MG TABLET;ORAL Discontinued None No No
GLIPIZIDE GLIPIZIDE 10MG 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
07/11/2006 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
03/31/2017 SUPPL-12 Labeling-Package Insert

Label is not available on this site.

06/17/2015 SUPPL-11 Labeling-Package Insert

Label is not available on this site.

08/17/2015 SUPPL-9 Labeling-Package Insert

Label is not available on this site.

08/17/2015 SUPPL-8 Labeling-Package Insert

Label is not available on this site.

03/23/2009 SUPPL-2 Labeling

Label is not available on this site.

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