FDA.reportPublic FDA data

Application 215585

Type
ANDA
Sponsor
RICONPHARMA LLC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DICLOFENAC POTASSIUMDICLOFENAC POTASSIUMTABLET;ORAL50MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
50742-279Diclofenac Potassiumdiclofenac potassiumIngenus Pharmaceuticals, LLCANDACurrent
50742-279Diclofenac Potassiumdiclofenac potassiumIngenus Pharmaceuticals, LLCANDACurrent
68071-2892Diclofenac Potassiumdiclofenac potassiumNuCare Pharmaceuticals,Inc.ANDACurrent
68071-2892Diclofenac Potassiumdiclofenac potassiumNuCare Pharmaceuticals,Inc.ANDACurrent
70518-3538Diclofenac Potassiumdiclofenac potassiumREMEDYREPACK INC.ANDACurrent
70518-3538Diclofenac Potassiumdiclofenac potassiumREMEDYREPACK INC.ANDACurrent