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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 065190
Company: ANI PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CEFUROXIME AXETIL CEFUROXIME AXETIL EQ 250MG BASE TABLET;ORAL Discontinued None No No
CEFUROXIME AXETIL CEFUROXIME AXETIL EQ 500MG BASE 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
10/18/2004 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
03/19/2020 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

03/19/2020 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

10/31/2007 SUPPL-3 Labeling

Label is not available on this site.

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