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=ANDA040230"
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
68071-4782-9 68071-4782 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20190222 N/A ANDA ANDA040230 NuCare Pharmaceuticals,Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (68071-4782-9)
68071-4782-1 68071-4782 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20190222 N/A ANDA ANDA040230 NuCare Pharmaceuticals,Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 10 TABLET in 1 BOTTLE (68071-4782-1)
68071-4782-3 68071-4782 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20190222 N/A ANDA ANDA040230 NuCare Pharmaceuticals,Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (68071-4782-3)
68071-4782-6 68071-4782 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20190222 N/A ANDA ANDA040230 NuCare Pharmaceuticals,Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 60 TABLET in 1 BOTTLE (68071-4782-6)
0904-6988-61 0904-6988 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 19990226 N/A ANDA ANDA040230 Major Pharmaceuticals DICYCLOMINE HYDROCHLORIDE 20 mg/1 100 BLISTER PACK in 1 CARTON (0904-6988-61) / 1 TABLET in 1 BLISTER PACK
71335-0425-4 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20200326 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (71335-0425-4)
71335-0425-5 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20180504 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 20 TABLET in 1 BOTTLE (71335-0425-5)
71335-0425-6 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20211227 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 21 TABLET in 1 BOTTLE (71335-0425-6)
71335-0425-7 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20211227 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 120 TABLET in 1 BOTTLE (71335-0425-7)
71335-0425-8 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20211227 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE (71335-0425-8)
71335-0425-9 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20200601 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 28 TABLET in 1 BOTTLE (71335-0425-9)
71335-0425-1 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20180222 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (71335-0425-1)
71335-0425-2 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20211227 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 40 TABLET in 1 BOTTLE (71335-0425-2)
71335-0425-3 71335-0425 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20201112 N/A ANDA ANDA040230 Bryant Ranch Prepack DICYCLOMINE HYDROCHLORIDE 20 mg/1 60 TABLET in 1 BOTTLE (71335-0425-3)
51655-940-26 51655-940 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20210715 N/A ANDA ANDA040230 Northwind Pharmaceuticals DICYCLOMINE HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-940-26)
0527-1282-01 0527-1282 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 19990226 N/A ANDA ANDA040230 Lannett Company, Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE (0527-1282-01)
0527-1282-05 0527-1282 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 19990226 N/A ANDA ANDA040230 Lannett Company, Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 500 TABLET in 1 BOTTLE (0527-1282-05)
70518-1767-0 70518-1767 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20190102 N/A ANDA ANDA040230 REMEDYREPACK INC. DICYCLOMINE HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BLISTER PACK (70518-1767-0)
70518-1767-2 70518-1767 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 20230802 N/A ANDA ANDA040230 REMEDYREPACK INC. DICYCLOMINE HYDROCHLORIDE 20 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (70518-1767-2)
0527-1282-10 0527-1282 HUMAN PRESCRIPTION DRUG Dicyclomine Hydrochloride Dicyclomine Hydrochloride TABLET ORAL 19990226 N/A ANDA ANDA040230 Lannett Company, Inc. DICYCLOMINE HYDROCHLORIDE 20 mg/1 1000 TABLET in 1 BOTTLE (0527-1282-10)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase