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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 200835
Company: WATSON LABS INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BUPROPION HYDROBROMIDE BUPROPION HYDROBROMIDE 174MG TABLET, EXTENDED RELEASE; ORAL None (Tentative Approval) None No No
BUPROPION HYDROBROMIDE BUPROPION HYDROBROMIDE 522MG TABLET, EXTENDED RELEASE; 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
08/13/2013 ORIG-1 Tentative Approval Not Applicable

Label is not available on this site.

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