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=NDA020989"
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
63395-201-13 63395-201 HUMAN PRESCRIPTION DRUG Evoxac cevimeline hydrochloride CAPSULE ORAL 20000112 20250831 NDA NDA020989 Daiichi Sankyo, Inc. CEVIMELINE HYDROCHLORIDE 30 mg/1 100 CAPSULE in 1 BOTTLE, PLASTIC (63395-201-13)
63304-479-01 63304-479 HUMAN PRESCRIPTION DRUG Cevimeline Cevimeline CAPSULE ORAL 20160310 20270430 NDA NDA020989 Sun Pharmaceutical Industries, Inc. CEVIMELINE HYDROCHLORIDE 30 mg/1 100 CAPSULE in 1 BOTTLE (63304-479-01)
0713-0937-01 0713-0937 HUMAN PRESCRIPTION DRUG cevimeline hydrochloride cevimeline hydrochloride CAPSULE ORAL 20230103 N/A NDA NDA020989 Cosette Pharmaceuticals, Inc. CEVIMELINE HYDROCHLORIDE 30 mg/1 100 CAPSULE in 1 BOTTLE, PLASTIC (0713-0937-01)
0713-0883-01 0713-0883 HUMAN PRESCRIPTION DRUG Evoxac cevimeline hydrochloride CAPSULE ORAL 20220901 N/A NDA NDA020989 Cosette Pharmaceuticals, Inc. CEVIMELINE HYDROCHLORIDE 30 mg/1 100 CAPSULE in 1 BOTTLE, PLASTIC (0713-0883-01)
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