Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 211566
Company: ZYDUS LIFESCIENCES
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 |