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
70771-1145-0	70771-1145	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1145-0)
70771-1145-1	70771-1145	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1145-1)
70771-1145-3	70771-1145	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1145-3)
70771-1145-5	70771-1145	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1145-5)
70771-1145-9	70771-1145	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1145-9)
70771-1146-0	70771-1146	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1146-0)
70771-1146-1	70771-1146	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1146-1)
70771-1146-3	70771-1146	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1146-3)
70771-1146-5	70771-1146	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1146-5)
70771-1146-9	70771-1146	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1146-9)
70771-1147-0	70771-1147	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1147-0)
70771-1147-1	70771-1147	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1147-1)
70771-1147-3	70771-1147	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1147-3)
70771-1147-5	70771-1147	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1147-5)
70771-1147-9	70771-1147	HUMAN PRESCRIPTION DRUG	escitalopram	escitalopram	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA077734	Zydus Lifesciences Limited	ESCITALOPRAM OXALATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1147-9)