FDA.reportPublic FDA data

Application 076831

Type
ANDA
Sponsor
PADDOCK LLC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001FLAVOXATE HYDROCHLORIDEFLAVOXATE HYDROCHLORIDETABLET;ORAL100MGNoYes

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0574-0115FLAVOXATE HYDROCHLORIDEFLAVOXATE HYDROCHLORIDEPaddock Laboratories, LLCANDACurrent
0574-0115FLAVOXATE HYDROCHLORIDEFLAVOXATE HYDROCHLORIDEPadagis US LLCANDACurrent
0574-0115FLAVOXATE HYDROCHLORIDEFLAVOXATE HYDROCHLORIDEPadagis US LLCANDACurrent
68151-3826FLAVOXATE HYDROCHLORIDEFLAVOXATE HYDROCHLORIDECarilion Materials ManagementANDACurrent