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=NDA021908"
符合检索条件的记录共 61 条，共 4 页，当前第 2 页 ，可点击列名称排序
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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
71205-832-72 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 120 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-72)
71205-832-78 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 180 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-78)
71205-832-90 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-90)
71205-834-00 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-00)
71205-834-11 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 1000 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-11)
71205-834-30 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 30 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-30)
71205-834-55 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-55)
71205-834-60 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-60)
71205-834-64 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 240 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-64)
71205-834-67 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 270 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-67)
71205-834-72 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 120 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-72)
71205-834-78 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 180 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-78)
71205-834-90 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-90)
71205-831-30 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 30 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-30)
71205-831-55 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-55)
71205-831-00 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-00)
63304-351-60 63304-351 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230101 N/A NDA AUTHORIZED GENERIC NDA021908 Sun Pharmaceutical Industries, Inc. LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-351-60)
63304-352-60 63304-352 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230101 N/A NDA AUTHORIZED GENERIC NDA021908 Sun Pharmaceutical Industries, Inc. LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-352-60)
69339-162-17 69339-162 HUMAN PRESCRIPTION DRUG LUBIPROSTONE LUBIPROSTONE CAPSULE ORAL 20221017 N/A NDA AUTHORIZED GENERIC NDA021908 Natco Pharma USA LLC LUBIPROSTONE 8 ug/1 40 BLISTER PACK in 1 CARTON (69339-162-17) / 1 CAPSULE in 1 BLISTER PACK (69339-162-98)
69339-163-17 69339-163 HUMAN PRESCRIPTION DRUG LUBIPROSTONE LUBIPROSTONE CAPSULE ORAL 20221017 N/A NDA AUTHORIZED GENERIC NDA021908 Natco Pharma USA LLC LUBIPROSTONE 24 ug/1 40 BLISTER PACK in 1 CARTON (69339-163-17) / 1 CAPSULE in 1 BLISTER PACK (69339-163-98)
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