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）

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
58151-155-77	58151-155	HUMAN PRESCRIPTION DRUG	Lipitor	atorvastatin calcium	TABLET, FILM COATED	ORAL	20240501	N/A	NDA	NDA020702	Viatris Specialty LLC	ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (58151-155-77)
58151-156-77	58151-156	HUMAN PRESCRIPTION DRUG	Lipitor	atorvastatin calcium	TABLET, FILM COATED	ORAL	20240220	N/A	NDA	NDA020702	Viatris Specialty LLC	ATORVASTATIN CALCIUM TRIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (58151-156-77)
58151-157-77	58151-157	HUMAN PRESCRIPTION DRUG	Lipitor	atorvastatin calcium	TABLET, FILM COATED	ORAL	20240103	N/A	NDA	NDA020702	Viatris Specialty LLC	ATORVASTATIN CALCIUM TRIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (58151-157-77)
58151-158-77	58151-158	HUMAN PRESCRIPTION DRUG	Lipitor	atorvastatin calcium	TABLET, FILM COATED	ORAL	20240229	N/A	NDA	NDA020702	Viatris Specialty LLC	ATORVASTATIN CALCIUM TRIHYDRATE	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (58151-158-77)
0071-0155-23	0071-0155	HUMAN PRESCRIPTION DRUG	Lipitor	atorvastatin calcium	TABLET, FILM COATED	ORAL	19961217	20250430	NDA	NDA020702	Parke-Davis Div of Pfizer Inc	ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0071-0155-23)
0071-0156-23	0071-0156	HUMAN PRESCRIPTION DRUG	Lipitor	atorvastatin calcium	TABLET, FILM COATED	ORAL	19961217	20250930	NDA	NDA020702	Parke-Davis Div of Pfizer Inc	ATORVASTATIN CALCIUM TRIHYDRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0071-0156-23)
0071-0157-23	0071-0157	HUMAN PRESCRIPTION DRUG	Lipitor	atorvastatin calcium	TABLET, FILM COATED	ORAL	19961217	20260331	NDA	NDA020702	Parke-Davis Div of Pfizer Inc	ATORVASTATIN CALCIUM TRIHYDRATE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0071-0157-23)
0071-0158-23	0071-0158	HUMAN PRESCRIPTION DRUG	Lipitor	atorvastatin calcium	TABLET, FILM COATED	ORAL	20000407	20250930	NDA	NDA020702	Parke-Davis Div of Pfizer Inc	ATORVASTATIN CALCIUM TRIHYDRATE	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0071-0158-23)