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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 040826
Company: SUN PHARM INDS LTD
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHEN; HYDROCODONE BITARTRATE 325MG;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
08/16/2007 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
12/15/2023 SUPPL-14 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

12/15/2023 SUPPL-13 Labeling-Package Insert

Label is not available on this site.

03/04/2021 SUPPL-12 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

10/11/2019 SUPPL-11 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

09/21/2018 SUPPL-10 Labeling-Package Insert

Label is not available on this site.

09/18/2018 SUPPL-9 REMS - PROPOSAL - D-N-A

Label is not available on this site.

03/23/2017 SUPPL-8 Labeling-Package Insert

Label is not available on this site.

12/16/2016 SUPPL-7 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

12/16/2016 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

12/15/2016 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

04/04/2014 SUPPL-4 Labeling-Package Insert

Label is not available on this site.

06/27/2011 SUPPL-3 Labeling-Package Insert

Label is not available on this site.

05/09/2008 SUPPL-1 Labeling

Label is not available on this site.

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