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=ANDA040161"
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
67296-1741-1 67296-1741 HUMAN PRESCRIPTION DRUG Dicyclomine Dicyclomine hydrochloride TABLET ORAL 20200101 N/A ANDA ANDA040161 RedPharm Drug, Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 10 TABLET in 1 BOTTLE (67296-1741-1)
67296-1741-7 67296-1741 HUMAN PRESCRIPTION DRUG Dicyclomine Dicyclomine hydrochloride TABLET ORAL 20200101 N/A ANDA ANDA040161 RedPharm Drug, Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 15 TABLET in 1 BOTTLE (67296-1741-7)
68071-3782-3 68071-3782 HUMAN PRESCRIPTION DRUG Dicyclomine Dicyclomine hydrochloride TABLET ORAL 20250123 N/A ANDA ANDA040161 NuCare Pharmaceuticals, Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (68071-3782-3)
68071-3782-6 68071-3782 HUMAN PRESCRIPTION DRUG Dicyclomine Dicyclomine hydrochloride TABLET ORAL 20250224 N/A ANDA ANDA040161 NuCare Pharmaceuticals, Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (68071-3782-6)
0615-8561-39 0615-8561 HUMAN PRESCRIPTION DRUG Dicyclomine Dicyclomine hydrochloride TABLET ORAL 20250213 N/A ANDA ANDA040161 NCS HealthCare of KY, LLC dba Vangard Labs DICYCLOMINE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BLISTER PACK (0615-8561-39)
0143-1227-01 0143-1227 HUMAN PRESCRIPTION DRUG Dicyclomine Dicyclomine hydrochloride TABLET ORAL 19961001 N/A ANDA ANDA040161 Hikma Pharmaceuticals USA Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0143-1227-01)
0143-1227-10 0143-1227 HUMAN PRESCRIPTION DRUG Dicyclomine Dicyclomine hydrochloride TABLET ORAL 19961001 N/A ANDA ANDA040161 Hikma Pharmaceuticals USA Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (0143-1227-10)
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