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
71205-935-00	71205-935	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	25 mg/1	100 TABLET, COATED in 1 BOTTLE (71205-935-00)
71205-935-30	71205-935	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	25 mg/1	30 TABLET, COATED in 1 BOTTLE (71205-935-30)
71205-935-60	71205-935	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	25 mg/1	60 TABLET, COATED in 1 BOTTLE (71205-935-60)
71205-935-90	71205-935	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	25 mg/1	90 TABLET, COATED in 1 BOTTLE (71205-935-90)
71205-936-00	71205-936	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	50 mg/1	100 TABLET, COATED in 1 BOTTLE (71205-936-00)
71205-936-30	71205-936	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	50 mg/1	30 TABLET, COATED in 1 BOTTLE (71205-936-30)
71205-936-60	71205-936	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	50 mg/1	60 TABLET, COATED in 1 BOTTLE (71205-936-60)
71205-936-90	71205-936	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	50 mg/1	90 TABLET, COATED in 1 BOTTLE (71205-936-90)
71205-937-00	71205-937	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	100 mg/1	100 TABLET, COATED in 1 BOTTLE (71205-937-00)
71205-937-30	71205-937	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	100 mg/1	30 TABLET, COATED in 1 BOTTLE (71205-937-30)
71205-937-60	71205-937	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	100 mg/1	60 TABLET, COATED in 1 BOTTLE (71205-937-60)
71205-937-90	71205-937	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210301	N/A	ANDA	ANDA203965	Proficient Rx LP	MIGLITOL	100 mg/1	90 TABLET, COATED in 1 BOTTLE (71205-937-90)
69367-303-01	69367-303	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210115	N/A	ANDA	ANDA203965	Westminster Pharmaceuticals, LLC	MIGLITOL	25 mg/1	100 TABLET, COATED in 1 BOTTLE (69367-303-01)
69367-304-01	69367-304	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210115	N/A	ANDA	ANDA203965	Westminster Pharmaceuticals, LLC	MIGLITOL	50 mg/1	100 TABLET, COATED in 1 BOTTLE (69367-304-01)
69367-305-01	69367-305	HUMAN PRESCRIPTION DRUG	Miglitol	Miglitol	TABLET, COATED	ORAL	20210115	N/A	ANDA	ANDA203965	Westminster Pharmaceuticals, LLC	MIGLITOL	100 mg/1	100 TABLET, COATED in 1 BOTTLE (69367-305-01)