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=ANDA203083"
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
31722-571-10 31722-571 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20200518 N/A ANDA ANDA203083 Camber Pharmaceuticals, Inc. LANSOPRAZOLE 30 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-10)
31722-570-10 31722-570 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20200518 N/A ANDA ANDA203083 Camber Pharmaceuticals, Inc. LANSOPRAZOLE 15 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-570-10)
31722-570-30 31722-570 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20200518 N/A ANDA ANDA203083 Camber Pharmaceuticals, Inc. LANSOPRAZOLE 15 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-570-30)
31722-570-01 31722-570 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20200518 N/A ANDA ANDA203083 Camber Pharmaceuticals, Inc. LANSOPRAZOLE 15 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-570-01)
31722-571-30 31722-571 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20200518 N/A ANDA ANDA203083 Camber Pharmaceuticals, Inc. LANSOPRAZOLE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-30)
31722-571-90 31722-571 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20200518 N/A ANDA ANDA203083 Camber Pharmaceuticals, Inc. LANSOPRAZOLE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-571-90)
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