FDA.reportPublic FDA data

Application 214574

Type
ANDA
Sponsor
SUN PHARM INDS INC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001AMPHETAMINE SULFATEAMPHETAMINE SULFATETABLET;ORAL5MGNoNo
002AMPHETAMINE SULFATEAMPHETAMINE SULFATETABLET;ORAL10MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
57664-062Amphetamine SulfateAmphetamine SulfateSun Pharmaceutical Industries, Inc.ANDACurrent
57664-062Amphetamine SulfateAmphetamine SulfateSun Pharmaceutical Industries, Inc.ANDACurrent
57664-075Amphetamine SulfateAmphetamine SulfateSun Pharmaceutical Industries, Inc.ANDACurrent
57664-075Amphetamine SulfateAmphetamine SulfateSun Pharmaceutical Industries, Inc.ANDACurrent