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=ANDA218036"
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
68094-077-62 68094-077 HUMAN PRESCRIPTION DRUG Lithium Lithium Citrate SOLUTION ORAL 20251024 N/A ANDA ANDA218036 Precision Dose, Inc. LITHIUM CITRATE 8 meq/5mL 3 TRAY in 1 CASE (68094-077-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (68094-077-59)
72888-172-46 72888-172 HUMAN PRESCRIPTION DRUG Lithium Lithium SOLUTION ORAL 20221109 N/A ANDA ANDA218036 Advagen Pharma Ltd LITHIUM CITRATE 8 meq/5mL 500 mL in 1 BOTTLE (72888-172-46)
70518-4227-0 70518-4227 HUMAN PRESCRIPTION DRUG Lithium Lithium SOLUTION ORAL 20241104 N/A ANDA ANDA218036 REMEDYREPACK INC. LITHIUM CITRATE 8 meq/5mL 10 CUP in 1 BOX (70518-4227-0) / 5 mL in 1 CUP (70518-4227-1)
70518-4227-2 70518-4227 HUMAN PRESCRIPTION DRUG Lithium Lithium SOLUTION ORAL 20241105 N/A ANDA ANDA218036 REMEDYREPACK INC. LITHIUM CITRATE 8 meq/5mL 10 CUP, UNIT-DOSE in 1 BOX (70518-4227-2) / 10 mL in 1 CUP, UNIT-DOSE (70518-4227-3)
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