U.S. flag An official website of the United States government
  1. Home
  2. Drug Databases
  3. Drugs@FDA

Drugs@FDA: FDA-Approved Drugs

Home | Previous Page

Abbreviated New Drug Application (ANDA): 076635
Company: SUN PHARM INDS LTD
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
FENOFIBRATE FENOFIBRATE 54MG TABLET;ORAL Discontinued None No No
FENOFIBRATE FENOFIBRATE 107MG TABLET;ORAL Prescription None No No
FENOFIBRATE FENOFIBRATE 160MG 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
10/31/2005 ORIG-1 Approval Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/076635ltr.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
06/03/2021 SUPPL-15 Labeling-Package Insert

Label is not available on this site.

10/13/2020 SUPPL-13 Labeling-Package Insert

Label is not available on this site.

10/13/2020 SUPPL-11 Labeling-Package Insert

Label is not available on this site.

10/13/2020 SUPPL-10 Labeling-Package Insert

Label is not available on this site.

05/18/2018 SUPPL-9 Labeling-Container/Carton Labels, Labeling-Package Insert

Label is not available on this site.

Back to Top