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=ANDA076691"
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
0054-0020-25 0054-0020 HUMAN PRESCRIPTION DRUG Lithium Carbonate Lithium Carbonate TABLET, EXTENDED RELEASE ORAL 20040113 N/A ANDA ANDA076691 Hikma Pharmaceuticals USA Inc. LITHIUM CARBONATE 450 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0020-25)
43063-901-30 43063-901 HUMAN PRESCRIPTION DRUG Lithium Carbonate Lithium Carbonate TABLET, EXTENDED RELEASE ORAL 20230728 N/A ANDA ANDA076691 PD-Rx Pharmaceuticals, Inc. LITHIUM CARBONATE 450 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-901-30)
43063-901-01 43063-901 HUMAN PRESCRIPTION DRUG Lithium Carbonate Lithium Carbonate TABLET, EXTENDED RELEASE ORAL 20180925 N/A ANDA ANDA076691 PD-Rx Pharmaceuticals, Inc. LITHIUM CARBONATE 450 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-901-01)
68084-655-01 68084-655 HUMAN PRESCRIPTION DRUG Lithium Carbonate Lithium Carbonate TABLET, EXTENDED RELEASE ORAL 20140103 N/A ANDA ANDA076691 American Health Packaging LITHIUM CARBONATE 450 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-655-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-655-11)
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