FDA.reportPublic FDA data

Application 091418

Type
ANDA
Sponsor
SUN PHARM INDS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DOXORUBICIN HYDROCHLORIDEDOXORUBICIN HYDROCHLORIDEINJECTABLE;INJECTION2MG/MLNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
62756-826DOXOrubicin HydrochlorideDOXOrubicin HydrochlorideSun Pharmaceutical Industries, Inc.ANDACurrent
62756-826DOXOrubicin HydrochlorideDOXOrubicin HydrochlorideSun Pharmaceutical Industries, Inc.ANDACurrent
62756-827DOXOrubicin HydrochlorideDOXOrubicin HydrochlorideSun Pharmaceutical Industries, Inc.ANDACurrent
62756-827DOXOrubicin HydrochlorideDOXOrubicin HydrochlorideSun Pharmaceutical Industries, Inc.ANDACurrent