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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 019786
Company: NOVARTIS

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LOPRESSOR METOPROLOL FUMARATE EQ 100MG TARTRATE TABLET, EXTENDED RELEASE;ORAL Discontinued None No No
LOPRESSOR METOPROLOL FUMARATE EQ 200MG TARTRATE TABLET, EXTENDED RELEASE;ORAL Discontinued None No No
LOPRESSOR METOPROLOL FUMARATE EQ 300MG TARTRATE TABLET, EXTENDED RELEASE;ORAL Discontinued None No No
LOPRESSOR METOPROLOL FUMARATE EQ 400MG TARTRATE 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
12/27/1989 ORIG-1 Approval Type 2 - New Active Ingredient and Type 3 - New Dosage Form STANDARD

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