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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 075900
Company: CHARTWELL RX
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
FLUVOXAMINE MALEATE FLUVOXAMINE MALEATE 25MG TABLET;ORAL Discontinued None No No
FLUVOXAMINE MALEATE FLUVOXAMINE MALEATE 50MG TABLET;ORAL Discontinued None No No
FLUVOXAMINE MALEATE FLUVOXAMINE MALEATE 100MG 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
02/23/2006 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
04/15/2009 SUPPL-10 Labeling

Label is not available on this site.

02/27/2009 SUPPL-9 Labeling

Label is not available on this site.

10/16/2007 SUPPL-7 Labeling

Label is not available on this site.

07/09/2007 SUPPL-6 Labeling

Label is not available on this site.

10/18/2006 SUPPL-4 Labeling

Label is not available on this site.

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