Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 210240
Company: HETERO USA INC
Company: HETERO USA INC
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
ALOGLIPTIN | ALOGLIPTIN | 6.25MG | TABLET;ORAL | None (Tentative Approval) | None | No | No |
ALOGLIPTIN | ALOGLIPTIN | 12.5MG | TABLET;ORAL | None (Tentative Approval) | None | No | No |
ALOGLIPTIN | ALOGLIPTIN | 25MG | TABLET;ORAL | None (Tentative Approval) | 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 |
---|---|---|---|---|---|---|---|
08/28/2018 | ORIG-1 | Tentative Approval | STANDARD |
Letter (PDF)
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Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/210240Orig1s000TAltr.pdf |