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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 201748
Company: SUN PHARM INDS LTD
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
FENOFIBRATE (MICRONIZED) FENOFIBRATE 43MG CAPSULE;ORAL Discontinued None No No
FENOFIBRATE (MICRONIZED) FENOFIBRATE 130MG CAPSULE;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
10/31/2014 ORIG-1 Approval Not Applicable

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
05/22/2025 SUPPL-10 Labeling-Package Insert

Label is not available on this site.

05/22/2025 SUPPL-7 Labeling-Package Insert

Label is not available on this site.

08/25/2020 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

08/25/2020 SUPPL-4 Labeling-Package Insert

Label is not available on this site.

08/25/2020 SUPPL-3 Labeling-Package Insert

Label is not available on this site.

08/25/2020 SUPPL-2 Labeling-Container/Carton Labels, Labeling-Package Insert

Label is not available on this site.

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