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=ANDA214422"
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
31722-134-01 31722-134 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210120 N/A ANDA ANDA214422 Camber Pharmaceuticals, Inc. POTASSIUM CHLORIDE 1125 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-134-01)
31722-135-01 31722-135 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210120 N/A ANDA ANDA214422 Camber Pharmaceuticals, Inc. POTASSIUM CHLORIDE 1500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-135-01)
31722-135-05 31722-135 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210120 N/A ANDA ANDA214422 Camber Pharmaceuticals, Inc. POTASSIUM CHLORIDE 1500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-135-05)
72865-195-05 72865-195 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210304 N/A ANDA ANDA214422 XLCare Pharmaceuticals, Inc. POTASSIUM CHLORIDE 1125 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-195-05)
72865-196-01 72865-196 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210304 N/A ANDA ANDA214422 XLCare Pharmaceuticals, Inc. POTASSIUM CHLORIDE 1500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-196-01)
72865-196-05 72865-196 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210304 N/A ANDA ANDA214422 XLCare Pharmaceuticals, Inc. POTASSIUM CHLORIDE 1500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-196-05)
72865-195-01 72865-195 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210304 N/A ANDA ANDA214422 XLCare Pharmaceuticals, Inc. POTASSIUM CHLORIDE 1125 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-195-01)
72865-194-05 72865-194 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium CHLORIDE TABLET, EXTENDED RELEASE ORAL 20210304 N/A ANDA ANDA214422 XLCare Pharmaceuticals, Inc. POTASSIUM CHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-194-05)
72865-194-01 72865-194 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium CHLORIDE TABLET, EXTENDED RELEASE ORAL 20210304 N/A ANDA ANDA214422 XLCare Pharmaceuticals, Inc. POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-194-01)
50090-6253-0 50090-6253 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20221202 N/A ANDA ANDA214422 A-S Medication Solutions POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6253-0)
50090-6253-1 50090-6253 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20221202 N/A ANDA ANDA214422 A-S Medication Solutions POTASSIUM CHLORIDE 1500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6253-1)
50090-6253-2 50090-6253 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20221202 N/A ANDA ANDA214422 A-S Medication Solutions POTASSIUM CHLORIDE 1500 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6253-2)
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