FDA.reportPublic FDA data

Application 078690

Type
ANDA
Sponsor
SUN PHARM

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001CARBIDOPA AND LEVODOPACARBIDOPA; LEVODOPATABLET, ORALLY DISINTEGRATING;ORAL10MG;100MGNoNo
002CARBIDOPA AND LEVODOPACARBIDOPA; LEVODOPATABLET, ORALLY DISINTEGRATING;ORAL25MG;100MGNoNo
003CARBIDOPA AND LEVODOPACARBIDOPA; LEVODOPATABLET, ORALLY DISINTEGRATING;ORAL25MG;250MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
47335-186CARBIDOPA AND LEVODOPACARBIDOPA AND LEVODOPASun Pharmaceutical Industries, Inc.ANDACurrent
47335-187CARBIDOPA AND LEVODOPACARBIDOPA AND LEVODOPASun Pharmaceutical Industries, Inc.ANDACurrent
47335-188CARBIDOPA AND LEVODOPACARBIDOPA AND LEVODOPASun Pharmaceutical Industries, Inc.ANDACurrent