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=ANDA216848"
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
82137-016-01 82137-016 HUMAN PRESCRIPTION DRUG atorvastatin calcium atorvastatin calcium TABLET, FILM COATED ORAL 20221101 N/A ANDA ANDA216848 Lepu Pharmaceutical Technology Co., Ltd. ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82137-016-01)
82137-018-01 82137-018 HUMAN PRESCRIPTION DRUG atorvastatin calcium atorvastatin calcium TABLET, FILM COATED ORAL 20221101 N/A ANDA ANDA216848 Lepu Pharmaceutical Technology Co., Ltd. ATORVASTATIN CALCIUM TRIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82137-018-01)
82137-019-01 82137-019 HUMAN PRESCRIPTION DRUG atorvastatin calcium atorvastatin calcium TABLET, FILM COATED ORAL 20221101 N/A ANDA ANDA216848 Lepu Pharmaceutical Technology Co., Ltd. ATORVASTATIN CALCIUM TRIHYDRATE 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82137-019-01)
82137-017-01 82137-017 HUMAN PRESCRIPTION DRUG atorvastatin calcium atorvastatin calcium TABLET, FILM COATED ORAL 20221101 N/A ANDA ANDA216848 Lepu Pharmaceutical Technology Co., Ltd. ATORVASTATIN CALCIUM TRIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82137-017-01)
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