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
65862-662-30	65862-662	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	5 mg/1	30 TABLET in 1 BOTTLE (65862-662-30)
65862-662-78	65862-662	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	5 mg/1	10 BLISTER PACK in 1 CARTON (65862-662-78) / 10 TABLET in 1 BLISTER PACK (65862-662-10)
65862-663-01	65862-663	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	10 mg/1	100 TABLET in 1 BOTTLE (65862-663-01)
65862-663-05	65862-663	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	10 mg/1	500 TABLET in 1 BOTTLE (65862-663-05)
65862-663-30	65862-663	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	10 mg/1	30 TABLET in 1 BOTTLE (65862-663-30)
65862-663-78	65862-663	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	10 mg/1	10 BLISTER PACK in 1 CARTON (65862-663-78) / 10 TABLET in 1 BLISTER PACK (65862-663-10)
65862-664-01	65862-664	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	15 mg/1	100 TABLET in 1 BOTTLE (65862-664-01)
65862-664-05	65862-664	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	15 mg/1	500 TABLET in 1 BOTTLE (65862-664-05)
65862-664-30	65862-664	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	15 mg/1	30 TABLET in 1 BOTTLE (65862-664-30)
65862-664-78	65862-664	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	15 mg/1	10 BLISTER PACK in 1 CARTON (65862-664-78) / 10 TABLET in 1 BLISTER PACK (65862-664-10)
65862-665-01	65862-665	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	20 mg/1	100 TABLET in 1 BOTTLE (65862-665-01)
65862-665-05	65862-665	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	20 mg/1	500 TABLET in 1 BOTTLE (65862-665-05)
65862-665-30	65862-665	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	20 mg/1	30 TABLET in 1 BOTTLE (65862-665-30)
65862-665-78	65862-665	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	20 mg/1	10 BLISTER PACK in 1 CARTON (65862-665-78) / 10 TABLET in 1 BLISTER PACK (65862-665-10)
65862-666-01	65862-666	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	30 mg/1	100 TABLET in 1 BOTTLE (65862-666-01)
65862-666-05	65862-666	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	30 mg/1	500 TABLET in 1 BOTTLE (65862-666-05)
65862-666-30	65862-666	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	30 mg/1	30 TABLET in 1 BOTTLE (65862-666-30)
65862-666-78	65862-666	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20151008	N/A	ANDA	ANDA203908	Aurobindo Pharma Limited	ARIPIPRAZOLE	30 mg/1	10 BLISTER PACK in 1 CARTON (65862-666-78) / 10 TABLET in 1 BLISTER PACK (65862-666-10)
50090-6403-0	50090-6403	HUMAN PRESCRIPTION DRUG	Aripiprazole	Aripiprazole	TABLET	ORAL	20230322	N/A	ANDA	ANDA203908	A-S Medication Solutions	ARIPIPRAZOLE	20 mg/1	30 TABLET in 1 BOTTLE (50090-6403-0)