FDA.reportPublic FDA data

Application 081049

Type
ANDA
Sponsor
SUN PHARM INDUSTRIES

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001IMIPRAMINE HYDROCHLORIDEIMIPRAMINE HYDROCHLORIDETABLET;ORAL25MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
50090-0035Imipramine HydrochlorideImipramine HydrochlorideA-S Medication SolutionsANDACurrent
53489-331Imipramine HydrochlorideImipramine HydrochlorideSun Pharmaceutical Industries, Inc.ANDACurrent
54738-913Imipramine HydrochlorideImipramine HydrochlorideRichmond Pharmaceuticals, Inc.ANDACurrent