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=ANDA210200"
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
69543-451-10 69543-451 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride POWDER, FOR SOLUTION ORAL 20210101 N/A ANDA ANDA210200 Virtus Pharmaceuticals, LLC POTASSIUM CHLORIDE 1.5 g/1.77g 100 PACKET in 1 CARTON (69543-451-10) / 1.77 g in 1 PACKET (69543-451-01)
69543-451-30 69543-451 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride POWDER, FOR SOLUTION ORAL 20210101 N/A ANDA ANDA210200 Virtus Pharmaceuticals, LLC POTASSIUM CHLORIDE 1.5 g/1.77g 30 PACKET in 1 CARTON (69543-451-30) / 1.77 g in 1 PACKET (69543-451-01)
42806-094-01 42806-094 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE POWDER, FOR SOLUTION ORAL 20181128 N/A ANDA ANDA210200 Epic Pharma, LLC POTASSIUM CHLORIDE 1.5 g/1.77g 100 PACKET in 1 CARTON (42806-094-01) / 1.77 g in 1 PACKET (42806-094-99)
42806-094-30 42806-094 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE POWDER, FOR SOLUTION ORAL 20181128 N/A ANDA ANDA210200 Epic Pharma, LLC POTASSIUM CHLORIDE 1.5 g/1.77g 30 PACKET in 1 CARTON (42806-094-30) / 1.77 g in 1 PACKET (42806-094-99)
72162-2310-1 72162-2310 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride POWDER, FOR SOLUTION ORAL 20240507 N/A ANDA ANDA210200 Bryant Ranch Prepack POTASSIUM CHLORIDE 1.5 g/1.77g 100 PACKET in 1 CARTON (72162-2310-1) / 1.77 g in 1 PACKET (72162-2310-2)
72162-2310-3 72162-2310 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride POWDER, FOR SOLUTION ORAL 20240507 N/A ANDA ANDA210200 Bryant Ranch Prepack POTASSIUM CHLORIDE 1.5 g/1.77g 30 PACKET in 1 CARTON (72162-2310-3) / 1.77 g in 1 PACKET (72162-2310-4)
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