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=ANDA213413"
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
50090-5592-0 50090-5592 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20210712 N/A ANDA ANDA213413 A-S Medication Solutions ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 20 TABLET in 1 BOTTLE (50090-5592-0)
68071-2328-1 68071-2328 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20210111 N/A ANDA ANDA213413 NuCare Pharmaceuticals,Inc. ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 10 TABLET in 1 BOTTLE (68071-2328-1)
68071-2328-3 68071-2328 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20210111 N/A ANDA ANDA213413 NuCare Pharmaceuticals,Inc. ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 30 TABLET in 1 BOTTLE (68071-2328-3)
71335-1693-1 71335-1693 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20201013 N/A ANDA ANDA213413 Bryant Ranch Prepack ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 20 TABLET in 1 BOTTLE (71335-1693-1)
71335-1693-2 71335-1693 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20201210 N/A ANDA ANDA213413 Bryant Ranch Prepack ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 30 TABLET in 1 BOTTLE (71335-1693-2)
71335-1693-3 71335-1693 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20211229 N/A ANDA ANDA213413 Bryant Ranch Prepack ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 15 TABLET in 1 BOTTLE (71335-1693-3)
71335-1693-4 71335-1693 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20200903 N/A ANDA ANDA213413 Bryant Ranch Prepack ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 10 TABLET in 1 BOTTLE (71335-1693-4)
70518-3915-0 70518-3915 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20231116 N/A ANDA ANDA213413 REMEDYREPACK INC. ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 30 TABLET in 1 BLISTER PACK (70518-3915-0)
70518-3915-1 70518-3915 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20240624 N/A ANDA ANDA213413 REMEDYREPACK INC. ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 30 TABLET in 1 BLISTER PACK (70518-3915-1)
50090-5589-0 50090-5589 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20210712 N/A ANDA ANDA213413 A-S Medication Solutions ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 15 TABLET in 1 BOTTLE (50090-5589-0)
50090-5589-1 50090-5589 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20210712 N/A ANDA ANDA213413 A-S Medication Solutions ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 20 TABLET in 1 BOTTLE (50090-5589-1)
50090-5589-2 50090-5589 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20210712 N/A ANDA ANDA213413 A-S Medication Solutions ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 30 TABLET in 1 BOTTLE (50090-5589-2)
72189-336-10 72189-336 HUMAN PRESCRIPTION DRUG DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE TABLET ORAL 20220307 N/A ANDA ANDA213413 Direct Rx ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 10 TABLET in 1 BOTTLE (72189-336-10)
72189-336-30 72189-336 HUMAN PRESCRIPTION DRUG DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE TABLET ORAL 20220307 N/A ANDA ANDA213413 Direct Rx ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 30 TABLET in 1 BOTTLE (72189-336-30)
71335-1693-5 71335-1693 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20211229 N/A ANDA ANDA213413 Bryant Ranch Prepack ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 40 TABLET in 1 BOTTLE (71335-1693-5)
71335-1693-6 71335-1693 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20211229 N/A ANDA ANDA213413 Bryant Ranch Prepack ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 60 TABLET in 1 BOTTLE (71335-1693-6)
71335-1693-7 71335-1693 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20211229 N/A ANDA ANDA213413 Bryant Ranch Prepack ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 90 TABLET in 1 BOTTLE (71335-1693-7)
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