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=ANDA205868"
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
50090-6079-0 50090-6079 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20220919 N/A ANDA ANDA205868 A-S Medication Solutions LANSOPRAZOLE 15 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6079-0)
80425-0174-1 80425-0174 HUMAN PRESCRIPTION DRUG Lansoprazole DR Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20180604 N/A ANDA ANDA205868 Advanced Rx Pharmacy of Tennessee, LLC LANSOPRAZOLE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0174-1)
70756-807-30 70756-807 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20180604 N/A ANDA ANDA205868 Lifestar Pharma LLC. LANSOPRAZOLE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70756-807-30)
70756-807-51 70756-807 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20180604 N/A ANDA ANDA205868 Lifestar Pharma LLC. LANSOPRAZOLE 30 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70756-807-51)
70756-807-90 70756-807 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20180604 N/A ANDA ANDA205868 Lifestar Pharma LLC. LANSOPRAZOLE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70756-807-90)
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