FDA.reportPublic FDA data

Application 213588

Type
ANDA
Sponsor
CENTAUR PHARMS PVT

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001POTASSIUM CHLORIDEPOTASSIUM CHLORIDETABLET, EXTENDED RELEASE;ORAL10MEQNoNo
002POTASSIUM CHLORIDEPOTASSIUM CHLORIDETABLET, EXTENDED RELEASE;ORAL20MEQNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
64330-613Potassium ChloridePotassium ChlorideCentaur Pharmaceuticals Private LimitedANDACurrent
64330-613Potassium ChloridePotassium ChlorideCentaur Pharmaceuticals Private LimitedANDACurrent
64330-615Potassium ChloridePotassium ChlorideCentaur Pharmaceuticals Private LimitedANDACurrent
64330-615Potassium ChloridePotassium ChlorideCentaur Pharmaceuticals Private LimitedANDACurrent