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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 090941
Company: RISING
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE 150MG TABLET, EXTENDED RELEASE;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
05/03/2010 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
04/16/2024 SUPPL-15 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

04/16/2024 SUPPL-13 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

04/28/2017 SUPPL-10 Labeling-Package Insert

Label is not available on this site.

04/28/2017 SUPPL-9 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

11/20/2014 SUPPL-7 Labeling-Package Insert

Label is not available on this site.

11/20/2014 SUPPL-6 Labeling-Medication Guide

Label is not available on this site.

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