PRED FORTE (prednisolone-acetate) NDA 017011

by ALLERGAN

attributevalue
Drug NamePRED FORTE
Application Number017011
Active Ingredient(s)PREDNISOLONE ACETATE
CompanyALLERGAN
Dosages/Routes/Forms
Drug NameActive Ingredient(s)StrengthForm/RouteMarketing StatusRLDTE Code
PRED FORTEPREDNISOLONE ACETATE1%SUSPENSION/DROPS; OPHTHALMIC11AB
Approval History
DateSupplement No.ActionDocuments
Aug 03, 1995030Control Supplement
    Aug 05, 1975003Labeling Revision
      May 10, 1995031Control Supplement
        Nov 19, 1979011Control Supplement
          Dec 05, 1996032Control Supplement
            Jan 22, 1980012Manufacturing Change or Addition
              Sep 30, 1997033Control Supplement
                Sep 02, 1982013Manufacturing Change or Addition
                  May 19, 1998034Control Supplement
                    Sep 03, 1982014Manufacturing Change or Addition
                      Oct 02, 2000035Manufacturing Change or Addition
                        Jul 11, 1983016Package Change
                          Apr 12, 2001036Manufacturing Change or Addition
                            Aug 13, 1982017Control Supplement
                              Jul 24, 2001037Manufacturing Change or Addition
                                Apr 15, 1986021Labeling Revision
                                  Sep 28, 2001038Manufacturing Change or Addition
                                    Jun 13, 1986022Manufacturing Change or Addition
                                      Dec 04, 2001039Manufacturing Change or Addition
                                        Jun 13, 1986023Control Supplement
                                          Apr 30, 1987024Control Supplement
                                            Apr 12, 2002041Control Supplement
                                              Nov 03, 1987025Control Supplement
                                                Feb 17, 1988026Labeling Revision
                                                  Sep 09, 1988027Control Supplement
                                                    Oct 12, 1989028Manufacturing Change or Addition
                                                      May 30, 1973000Approval
                                                        Oct 30, 1989029Manufacturing Change or Addition
                                                          Nov 26, 1974001Control Supplement