FDA.reportPublic FDA data

Application 076835

Type
ANDA
Sponsor
EPIC PHARMA

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001FLAVOXATE HYDROCHLORIDEFLAVOXATE HYDROCHLORIDETABLET;ORAL100MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
24658-720Flavoxate HydrochlorideFlavoxate HydrochloridePuraCap Laboratories LLC dba Blu PharmaceuticalsANDACurrent
24658-720Flavoxate HydrochlorideFlavoxate HydrochloridePuraCap Laboratories LLC dba Blu PharmaceuticalsANDACurrent
42806-058Flavoxate HydrochlorideFlavoxate HydrochlorideEpic Pharma, LLCANDACurrent
50268-324Flavoxate HydrochlorideFlavoxate HydrochlorideAvPAKANDACurrent
51224-154Flavoxate HydrochlorideFlavoxate hydrochlorideTAGI Pharma, Inc.ANDACurrent
51224-154Flavoxate HydrochlorideFlavoxate hydrochlorideTAGI Pharma, Inc.ANDACurrent