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
11534-202-01	11534-202	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	2 mg/1	100 TABLET in 1 BOTTLE (11534-202-01)
11534-202-03	11534-202	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	2 mg/1	1000 TABLET in 1 BOTTLE (11534-202-03)
11534-202-04	11534-202	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	2 mg/1	500 TABLET in 1 BOTTLE (11534-202-04)
11534-199-01	11534-199	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	10 mg/1	100 TABLET in 1 BOTTLE (11534-199-01)
11534-199-03	11534-199	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	10 mg/1	1000 TABLET in 1 BOTTLE (11534-199-03)
11534-199-04	11534-199	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	10 mg/1	500 TABLET in 1 BOTTLE (11534-199-04)
11534-203-01	11534-203	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	5 mg/1	100 TABLET in 1 BOTTLE (11534-203-01)
11534-203-03	11534-203	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	5 mg/1	1000 TABLET in 1 BOTTLE (11534-203-03)
11534-203-04	11534-203	HUMAN PRESCRIPTION DRUG	DIAZEPAM	diazepam	TABLET	ORAL	20241210	N/A	ANDA	ANDA070464	Sunrise Pharmaceutical, Inc.	DIAZEPAM	5 mg/1	500 TABLET in 1 BOTTLE (11534-203-04)