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=NDA019123"
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
70518-3938-0 70518-3938 HUMAN PRESCRIPTION DRUG KLOR-CON potassium chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231206 N/A NDA NDA019123 REMEDYREPACK INC. POTASSIUM CHLORIDE 750 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3938-0)
70518-2313-2 70518-2313 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240926 N/A NDA NDA019123 REMEDYREPACK INC. POTASSIUM CHLORIDE 750 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2313-2)
0245-5315-01 0245-5315 HUMAN PRESCRIPTION DRUG KLOR-CON potassium chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190621 N/A NDA NDA019123 Upsher-Smith Laboratories, LLC POTASSIUM CHLORIDE 600 mg/1 100 BLISTER PACK in 1 BLISTER PACK (0245-5315-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0245-5315-89)
0245-5315-11 0245-5315 HUMAN PRESCRIPTION DRUG KLOR-CON potassium chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190621 N/A NDA NDA019123 Upsher-Smith Laboratories, LLC POTASSIUM CHLORIDE 600 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5315-11)
0245-5315-15 0245-5315 HUMAN PRESCRIPTION DRUG KLOR-CON potassium chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190621 N/A NDA NDA019123 Upsher-Smith Laboratories, LLC POTASSIUM CHLORIDE 600 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5315-15)
0832-5323-10 0832-5323 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190621 N/A NDA NDA019123 Upsher-Smith Laboratories, LLC POTASSIUM CHLORIDE 750 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-10)
0832-5323-11 0832-5323 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190621 N/A NDA NDA019123 Upsher-Smith Laboratories, LLC POTASSIUM CHLORIDE 750 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-11)
71610-349-15 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220208 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-15)
71610-349-30 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191016 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-30)
71610-349-45 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220208 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-45)
71610-349-53 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191016 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-53)
71610-349-60 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191016 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-60)
71610-349-70 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191016 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-70)
71610-349-80 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191016 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-80)
71610-349-85 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191016 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-85)
71610-349-92 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191016 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-92)
71610-349-94 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191016 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-94)
71610-349-98 71610-349 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220208 N/A NDA NDA019123 Aphena Pharma Solutions - Tennessee, LLC POTASSIUM CHLORIDE 750 mg/1 540 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-98)
0615-8318-05 0615-8318 HUMAN PRESCRIPTION DRUG Potassium Chloride potassium chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190930 20251130 NDA NDA019123 NCS HealthCare of KY, LLC dba Vangard Labs POTASSIUM CHLORIDE 750 mg/1 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8318-05)
0615-8318-14 0615-8318 HUMAN PRESCRIPTION DRUG Potassium Chloride potassium chloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190930 20251130 NDA NDA019123 NCS HealthCare of KY, LLC dba Vangard Labs POTASSIUM CHLORIDE 750 mg/1 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8318-14)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase