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
69315-910-10 69315-910 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20200315 N/A ANDA ANDA213413 Leading Pharma, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 1000 TABLET in 1 BOTTLE (69315-910-10)
67296-1485-9 67296-1485 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20200315 N/A ANDA ANDA213413 Redpharm Drug Inc. ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 100 TABLET in 1 BOTTLE (67296-1485-9)
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)
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)
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)
71610-809-60 71610-809 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20240322 N/A ANDA ANDA213413 Aphena Pharma Solutions - Tennessee, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 90 TABLET in 1 BOTTLE (71610-809-60)
71610-809-70 71610-809 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20240322 N/A ANDA ANDA213413 Aphena Pharma Solutions - Tennessee, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 120 TABLET in 1 BOTTLE (71610-809-70)
71205-909-90 71205-909 HUMAN PRESCRIPTION DRUG Diphenoxylate Hydrochloride and Atropine Sulfate diphenoxylate hydrochloride and atropine sulfate TABLET ORAL 20210716 N/A ANDA ANDA213413 Proficient Rx LP ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 90 TABLET in 1 BOTTLE (71205-909-90)
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