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=ANDA213441"
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
70771-1615-5 70771-1615 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20220210 N/A ANDA ANDA213441 Cadila Healthcare Limited NORTRIPTYLINE HYDROCHLORIDE 75 mg/1 500 CAPSULE in 1 BOTTLE (70771-1615-5)
70710-1156-1 70710-1156 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20220210 N/A ANDA ANDA213441 Zydus Pharmaceuticals (USA) Inc. NORTRIPTYLINE HYDROCHLORIDE 75 mg/1 100 CAPSULE in 1 BOTTLE (70710-1156-1)
70710-1156-3 70710-1156 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20220210 N/A ANDA ANDA213441 Zydus Pharmaceuticals (USA) Inc. NORTRIPTYLINE HYDROCHLORIDE 75 mg/1 30 CAPSULE in 1 BOTTLE (70710-1156-3)
70710-1156-5 70710-1156 HUMAN PRESCRIPTION DRUG Nortriptyline Hydrochloride Nortriptyline Hydrochloride CAPSULE ORAL 20220210 N/A ANDA ANDA213441 Zydus Pharmaceuticals (USA) Inc. NORTRIPTYLINE HYDROCHLORIDE 75 mg/1 500 CAPSULE in 1 BOTTLE (70710-1156-5)
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