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=ANDA200816"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
68382-771-77 68382-771 HUMAN PRESCRIPTION DRUG LANSOPRAZOLE LANSOPRAZOLE TABLET, ORALLY DISINTEGRATING ORAL 20181130 N/A ANDA ANDA200816 Zydus Pharmaceuticals USA Inc. LANSOPRAZOLE 15 mg/1 10 BLISTER PACK in 1 CARTON (68382-771-77) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-771-30)
68382-772-77 68382-772 HUMAN PRESCRIPTION DRUG LANSOPRAZOLE LANSOPRAZOLE TABLET, ORALLY DISINTEGRATING ORAL 20181130 N/A ANDA ANDA200816 Zydus Pharmaceuticals USA Inc. LANSOPRAZOLE 30 mg/1 10 BLISTER PACK in 1 CARTON (68382-772-77) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-772-30)
70771-1133-4 70771-1133 HUMAN PRESCRIPTION DRUG LANSOPRAZOLE LANSOPRAZOLE TABLET, ORALLY DISINTEGRATING ORAL 20181130 N/A ANDA ANDA200816 Zydus Lifesciences Limited LANSOPRAZOLE 30 mg/1 10 BLISTER PACK in 1 CARTON (70771-1133-4) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
70771-1132-4 70771-1132 HUMAN PRESCRIPTION DRUG LANSOPRAZOLE LANSOPRAZOLE TABLET, ORALLY DISINTEGRATING ORAL 20181130 N/A ANDA ANDA200816 Zydus Lifesciences Limited LANSOPRAZOLE 15 mg/1 10 BLISTER PACK in 1 CARTON (70771-1132-4) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
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