FDA.reportPublic FDA data

Application 203298

Type
ANDA
Sponsor
LOTUS PHARM CO LTD

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
10135-629Calcium AcetateCalcium AcetateMarlex Pharmaceuticals IncANDACurrent
10135-629Calcium AcetateCalcium AcetateMarlex Pharmaceuticals IncANDACurrent
40051-049Calcium AcetateCalcium AcetateLotus Pharmaceutical Co., Ltd. Nantou PlantANDACurrent
40051-049Calcium AcetateCalcium AcetateLotus Pharmaceutical Co., Ltd. Nantou PlantANDACurrent
51293-825Calcium AcetateCalcium AcetateECI Pharmaceuticals, LLCANDACurrent
51293-825Calcium AcetateCalcium AcetateECI Pharmaceuticals, LLCANDACurrent