FDA.reportPublic FDA data

Application 091312

Type
ANDA
Sponsor
CHARTWELL RX

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001CALCIUM ACETATECALCIUM ACETATECAPSULE;ORAL667MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
17856-0191Calcium AcetateCalcium AcetateATLANTIC BIOLOGICALS CORP.ANDACurrent
62135-191Calcium AcetateCalcium AcetateChartwell RX, LLC.ANDACurrent
62135-191Calcium AcetateCalcium AcetateChartwell RX, LLC.ANDACurrent
62135-191Calcium AcetateCalcium AcetateChartwell RX, LLC.ANDACurrent
68094-044Calcium AcetateCalcium AcetatePrecision Dose, Inc.ANDACurrent
70518-2723Calcium AcetateCalcium AcetateREMEDYREPACK INC.ANDACurrent
70518-2723Calcium AcetateCalcium AcetateREMEDYREPACK INC.ANDACurrent
70518-2723Calcium AcetateCalcium AcetateREMEDYREPACK INC.ANDACurrent