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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 210152
Company: BIONPHARMA INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
APIXABAN APIXABAN 2.5MG TABLET;ORAL Discontinued None No No
APIXABAN APIXABAN 5MG 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
04/08/2020 ORIG-1 Approval STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
05/20/2022 SUPPL-2 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

05/20/2022 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

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