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=ANDA090702"
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
71335-0120-1 71335-0120 HUMAN PRESCRIPTION DRUG lithium carbonate lithium carbonate CAPSULE ORAL 20211216 N/A ANDA ANDA090702 Bryant Ranch Prepack LITHIUM CARBONATE 300 mg/1 60 CAPSULE in 1 BOTTLE (71335-0120-1)
71335-0120-2 71335-0120 HUMAN PRESCRIPTION DRUG lithium carbonate lithium carbonate CAPSULE ORAL 20211216 N/A ANDA ANDA090702 Bryant Ranch Prepack LITHIUM CARBONATE 300 mg/1 100 CAPSULE in 1 BOTTLE (71335-0120-2)
71335-0120-3 71335-0120 HUMAN PRESCRIPTION DRUG lithium carbonate lithium carbonate CAPSULE ORAL 20211216 N/A ANDA ANDA090702 Bryant Ranch Prepack LITHIUM CARBONATE 300 mg/1 30 CAPSULE in 1 BOTTLE (71335-0120-3)
71335-0120-4 71335-0120 HUMAN PRESCRIPTION DRUG lithium carbonate lithium carbonate CAPSULE ORAL 20211216 N/A ANDA ANDA090702 Bryant Ranch Prepack LITHIUM CARBONATE 300 mg/1 90 CAPSULE in 1 BOTTLE (71335-0120-4)
71335-0120-5 71335-0120 HUMAN PRESCRIPTION DRUG lithium carbonate lithium carbonate CAPSULE ORAL 20211216 N/A ANDA ANDA090702 Bryant Ranch Prepack LITHIUM CARBONATE 300 mg/1 120 CAPSULE in 1 BOTTLE (71335-0120-5)
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