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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 200831
Company: WATSON LABS INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
EZETIMIBE EZETIMIBE 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
06/12/2017 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
08/02/2024 SUPPL-6 Labeling-Package Insert, Labeling-Patient Package Insert

Label is not available on this site.

08/02/2024 SUPPL-5 Labeling-Patient Package Insert, Labeling-Package Insert, Labeling-Container/Carton Labels

Label is not available on this site.

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