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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 218971
Company: MANKIND PHARMA LTD
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
SITAGLIPTIN AND METFORMIN HCL SITAGLIPTIN, METFORMIN HYDROCHLORIDE 1000MG ER TABLET TABLET None (Tentative Approval) None No No
SITAGLIPTIN AND METFORMIN HCL SITAGLIPTIN, METFORMIN HYDROCHLORIDE EQ 100MG BASE TABLET TABLET None (Tentative Approval) None No No
SITAGLIPTIN AND METFORMIN HCL SITAGLIPTIN, METFORMIN HYDROCHLORIDE 500MG TABLET None (Tentative Approval) None No No
SITAGLIPTIN AND METFORMIN HCL SITAGLIPTIN, METFORMIN HYDROCHLORIDE 50MG TABLET None (Tentative Approval) None No No
SITAGLIPTIN AND METFORMIN HCL SITAGLIPTIN, METFORMIN HYDROCHLORIDE 1000MG TABLET 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
12/11/2024 ORIG-1 Tentative Approval STANDARD Letter (PDF)

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https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/218971Orig1s000TAltr.pdf
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