美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA210733"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
64380-860-07 64380-860 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20181127 N/A ANDA ANDA210733 Strides Pharma Science Limited POTASSIUM CHLORIDE 600 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-07)
64380-860-08 64380-860 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20181127 N/A ANDA ANDA210733 Strides Pharma Science Limited POTASSIUM CHLORIDE 600 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-08)
64380-861-06 64380-861 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20181127 N/A ANDA ANDA210733 Strides Pharma Science Limited POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-06)
64380-861-07 64380-861 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20181127 N/A ANDA ANDA210733 Strides Pharma Science Limited POTASSIUM CHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-07)
64380-861-08 64380-861 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20181127 N/A ANDA ANDA210733 Strides Pharma Science Limited POTASSIUM CHLORIDE 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-08)
72189-027-30 72189-027 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20191002 N/A ANDA ANDA210733 Direct_Rx POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-30)
72189-027-04 72189-027 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20191002 N/A ANDA ANDA210733 Direct_Rx POTASSIUM CHLORIDE 750 mg/1 4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-04)
64380-860-06 64380-860 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20181119 N/A ANDA ANDA210733 Strides Pharma Science Limited POTASSIUM CHLORIDE 600 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-06)
51655-706-52 51655-706 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210430 N/A ANDA ANDA210733 Northwind Pharmaceuticals POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-706-52)
71335-1131-2 71335-1131 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA210733 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-2)
71335-1131-3 71335-1131 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA210733 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-3)
71335-1131-4 71335-1131 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA210733 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-4)
71335-1131-5 71335-1131 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA210733 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-5)
71335-1131-6 71335-1131 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA210733 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-6)
71335-1131-7 71335-1131 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA210733 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-7)
53002-2034-0 53002-2034 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210101 N/A ANDA ANDA210733 RPK Pharmaceuticals, Inc. POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-2034-0)
53002-2034-3 53002-2034 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210101 N/A ANDA ANDA210733 RPK Pharmaceuticals, Inc. POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-2034-3)
71335-1131-1 71335-1131 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20190305 N/A ANDA ANDA210733 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-1)
53002-1039-2 53002-1039 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240101 N/A ANDA ANDA210733 RPK Pharmaceuticals, Inc. POTASSIUM CHLORIDE 600 mg/1 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, DROPPER (53002-1039-2)
53002-1039-3 53002-1039 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240101 N/A ANDA ANDA210733 RPK Pharmaceuticals, Inc. POTASSIUM CHLORIDE 600 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, DROPPER (53002-1039-3)
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