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
71335-9693-5 71335-9693 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20230418 N/A ANDA ANDA203083 Bryant Ranch Prepack LANSOPRAZOLE 15 mg/1 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-5)
71335-9693-6 71335-9693 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20230418 N/A ANDA ANDA203083 Bryant Ranch Prepack LANSOPRAZOLE 15 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-6)
71335-9693-7 71335-9693 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20230418 N/A ANDA ANDA203083 Bryant Ranch Prepack LANSOPRAZOLE 15 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-7)
71335-9693-8 71335-9693 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20230418 N/A ANDA ANDA203083 Bryant Ranch Prepack LANSOPRAZOLE 15 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-8)
82009-039-05 82009-039 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole CAPSULE, DELAYED RELEASE ORAL 20221014 N/A ANDA ANDA203083 Quallent Pharmaceuticals Health LLC LANSOPRAZOLE 30 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-039-05)
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