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=ANDA085372"
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
0527-1170-10 0527-1170 HUMAN PRESCRIPTION DRUG DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE TABLET ORAL 19780221 N/A ANDA ANDA085372 Lannett Company, Inc. ATROPINE; DIPHENOXYLATE .025 mg/1; 2.5 mg/1 1000 TABLET in 1 BOTTLE (0527-1170-10)
0527-1170-05 0527-1170 HUMAN PRESCRIPTION DRUG DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE TABLET ORAL 19780221 N/A ANDA ANDA085372 Lannett Company, Inc. ATROPINE; DIPHENOXYLATE .025 mg/1; 2.5 mg/1 500 TABLET in 1 BOTTLE (0527-1170-05)
0527-1170-01 0527-1170 HUMAN PRESCRIPTION DRUG DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE TABLET ORAL 19780221 N/A ANDA ANDA085372 Lannett Company, Inc. ATROPINE; DIPHENOXYLATE .025 mg/1; 2.5 mg/1 100 TABLET in 1 BOTTLE (0527-1170-01)
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