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
70377-069-11	70377-069	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20250602	N/A	ANDA	ANDA216140	Biocon Pharma Inc.	EVEROLIMUS	.25 mg/1	60 TABLET in 1 BOTTLE (70377-069-11)
70377-069-12	70377-069	HUMAN PRESCRIPTION DRUG	Everolimus	Everolimus	TABLET	ORAL	20250602	N/A	ANDA	ANDA216140	Biocon Pharma Inc.	EVEROLIMUS	.25 mg/1	6 BLISTER PACK in 1 CARTON (70377-069-12) / 10 TABLET in 1 BLISTER PACK
70377-071-11	70377-071	HUMAN PRESCRIPTION DRUG	Everolimus	everolimus	TABLET	ORAL	20250602	N/A	ANDA	ANDA216140	Biocon Pharma Inc.	EVEROLIMUS	.75 mg/1	60 TABLET in 1 BOTTLE (70377-071-11)
70377-071-12	70377-071	HUMAN PRESCRIPTION DRUG	Everolimus	everolimus	TABLET	ORAL	20250602	N/A	ANDA	ANDA216140	Biocon Pharma Inc.	EVEROLIMUS	.75 mg/1	6 BLISTER PACK in 1 CARTON (70377-071-12) / 10 TABLET in 1 BLISTER PACK
70377-070-11	70377-070	HUMAN PRESCRIPTION DRUG	Everolimus	EVEROLIMUS	TABLET	ORAL	20250602	N/A	ANDA	ANDA216140	Biocon Pharma Inc.	EVEROLIMUS	.5 mg/1	60 TABLET in 1 BOTTLE (70377-070-11)
70377-070-21	70377-070	HUMAN PRESCRIPTION DRUG	Everolimus	EVEROLIMUS	TABLET	ORAL	20250602	N/A	ANDA	ANDA216140	Biocon Pharma Inc.	EVEROLIMUS	.5 mg/1	6 BLISTER PACK in 1 CARTON (70377-070-21) / 10 TABLET in 1 BLISTER PACK
70377-112-11	70377-112	HUMAN PRESCRIPTION DRUG	Everolimus	everolimus	TABLET	ORAL	20250602	N/A	ANDA	ANDA216140	Biocon Pharma Inc.	EVEROLIMUS	1 mg/1	60 TABLET in 1 BOTTLE (70377-112-11)
70377-112-21	70377-112	HUMAN PRESCRIPTION DRUG	Everolimus	everolimus	TABLET	ORAL	20250602	N/A	ANDA	ANDA216140	Biocon Pharma Inc.	EVEROLIMUS	1 mg/1	6 BLISTER PACK in 1 CARTON (70377-112-21) / 10 TABLET in 1 BLISTER PACK