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=ANDA211933"
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
70518-3273-6 70518-3273 HUMAN PRESCRIPTION DRUG Atorvastatin calcium Atorvastatin calcium TABLET, FILM COATED ORAL 20251019 N/A ANDA ANDA211933 REMEDYREPACK INC. ATORVASTATIN CALCIUM TRIHYDRATE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3273-6)
72189-557-30 72189-557 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20240614 N/A ANDA ANDA211933 Direct_rx ATORVASTATIN CALCIUM TRIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-557-30)
72189-557-90 72189-557 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20240614 N/A ANDA ANDA211933 Direct_rx ATORVASTATIN CALCIUM TRIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-557-90)
70518-3298-1 70518-3298 HUMAN PRESCRIPTION DRUG Atorvastatin calcium Atorvastatin calcium TABLET, FILM COATED ORAL 20240828 N/A ANDA ANDA211933 REMEDYREPACK INC. ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3298-1)
70518-3304-1 70518-3304 HUMAN PRESCRIPTION DRUG Atorvastatin calcium Atorvastatin calcium TABLET, FILM COATED ORAL 20221206 N/A ANDA ANDA211933 REMEDYREPACK INC. ATORVASTATIN CALCIUM TRIHYDRATE 80 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3304-1)
70518-3339-1 70518-3339 HUMAN PRESCRIPTION DRUG Atorvastatin calcium Atorvastatin calcium TABLET, FILM COATED ORAL 20231219 N/A ANDA ANDA211933 REMEDYREPACK INC. ATORVASTATIN CALCIUM TRIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3339-1)
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