FDA.reportPublic FDA data

Application 091027

Type
ANDA
Sponsor
SUN PHARM INDS INC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001LITHIUM CARBONATELITHIUM CARBONATETABLET;ORAL300MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
62756-430Lithium CarbonateLithium CarbonateSun Pharmaceutical Industries, Inc.ANDACurrent
62756-430Lithium CarbonateLithium CarbonateSun Pharmaceutical Industries, Inc.ANDACurrent
70518-1567Lithium CarbonateLithium CarbonateREMEDYREPACK INC.ANDACurrent
70518-1567Lithium CarbonateLithium CarbonateREMEDYREPACK INC.ANDACurrent
70518-1567Lithium CarbonateLithium CarbonateREMEDYREPACK INC.ANDACurrent
70518-2699Lithium CarbonateLithium CarbonateREMEDYREPACK INC.ANDACurrent
70518-2699Lithium CarbonateLithium CarbonateREMEDYREPACK INC.ANDACurrent
70518-2699Lithium CarbonateLithium CarbonateREMEDYREPACK INC.ANDACurrent
70518-2699Lithium CarbonateLithium CarbonateREMEDYREPACK INC.ANDACurrent