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=ANDA210571"
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
71610-566-30 71610-566 HUMAN PRESCRIPTION DRUG Diphenoxylate hydrochloride and atropine sulfate Diphenoxylate hydrochloride and Atropine sulfate TABLET ORAL 20210715 N/A ANDA ANDA210571 Aphena Pharma Solutions - Tennessee, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 30 TABLET in 1 BOTTLE (71610-566-30)
71610-566-53 71610-566 HUMAN PRESCRIPTION DRUG Diphenoxylate hydrochloride and atropine sulfate Diphenoxylate hydrochloride and Atropine sulfate TABLET ORAL 20210609 N/A ANDA ANDA210571 Aphena Pharma Solutions - Tennessee, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 60 TABLET in 1 BOTTLE (71610-566-53)
71610-566-60 71610-566 HUMAN PRESCRIPTION DRUG Diphenoxylate hydrochloride and atropine sulfate Diphenoxylate hydrochloride and Atropine sulfate TABLET ORAL 20210609 N/A ANDA ANDA210571 Aphena Pharma Solutions - Tennessee, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 90 TABLET in 1 BOTTLE (71610-566-60)
71610-566-70 71610-566 HUMAN PRESCRIPTION DRUG Diphenoxylate hydrochloride and atropine sulfate Diphenoxylate hydrochloride and Atropine sulfate TABLET ORAL 20210609 N/A ANDA ANDA210571 Aphena Pharma Solutions - Tennessee, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 120 TABLET in 1 BOTTLE (71610-566-70)
71610-566-80 71610-566 HUMAN PRESCRIPTION DRUG Diphenoxylate hydrochloride and atropine sulfate Diphenoxylate hydrochloride and Atropine sulfate TABLET ORAL 20210609 N/A ANDA ANDA210571 Aphena Pharma Solutions - Tennessee, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 180 TABLET in 1 BOTTLE (71610-566-80)
71610-566-90 71610-566 HUMAN PRESCRIPTION DRUG Diphenoxylate hydrochloride and atropine sulfate Diphenoxylate hydrochloride and Atropine sulfate TABLET ORAL 20210609 N/A ANDA ANDA210571 Aphena Pharma Solutions - Tennessee, LLC ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE .025 mg/1; 2.5 mg/1 240 TABLET in 1 BOTTLE (71610-566-90)
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