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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 211566
Company: ZYDUS LIFESCIENCES
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ZITUVIO SITAGLIPTIN 25MG TABLET;ORAL Prescription None Yes No
ZITUVIO SITAGLIPTIN 50MG TABLET;ORAL Prescription None Yes No
ZITUVIO SITAGLIPTIN 100MG TABLET;ORAL Prescription None Yes Yes
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
10/18/2023 ORIG-1 Approval Type 2 - New Active Ingredient STANDARD Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/211566s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/211566Orig1s000ltr.pdf
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
10/18/2023 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/211566s000lbl.pdf
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