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=ANDA040317"
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
71335-2341-1 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (71335-2341-1)
71335-2341-2 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 40 TABLET in 1 BOTTLE (71335-2341-2)
71335-2341-3 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 60 TABLET in 1 BOTTLE (71335-2341-3)
71335-2341-4 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (71335-2341-4)
71335-2341-5 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 20 TABLET in 1 BOTTLE (71335-2341-5)
71335-2341-6 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 21 TABLET in 1 BOTTLE (71335-2341-6)
71335-2341-7 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 120 TABLET in 1 BOTTLE (71335-2341-7)
71335-2341-8 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE (71335-2341-8)
71335-2341-9 71335-2341 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 28 TABLET in 1 BOTTLE (71335-2341-9)
68788-8581-3 68788-8581 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20240206 N/A ANDA ANDA040317 Preferred Pharmaceuticals Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (68788-8581-3)
59651-720-01 59651-720 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20230425 N/A ANDA ANDA040317 Aurobindo Pharma Limited DICYCLOMINE HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE (59651-720-01)
59651-720-99 59651-720 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20230425 N/A ANDA ANDA040317 Aurobindo Pharma Limited DICYCLOMINE HYDROCHLORIDE 20 mg/1 1000 TABLET in 1 BOTTLE (59651-720-99)
68071-3555-3 68071-3555 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20231221 N/A ANDA ANDA040317 NuCare Pharmaceuticals,Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (68071-3555-3)
68071-3555-6 68071-3555 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20231221 N/A ANDA ANDA040317 NuCare Pharmaceuticals,Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 60 TABLET in 1 BOTTLE (68071-3555-6)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase