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
65862-554-30	65862-554	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20121119	N/A	ANDA	ANDA202261	Aurobindo Pharma Limited	MINOCYCLINE HYDROCHLORIDE	45 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-554-30)
65862-554-99	65862-554	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20121119	N/A	ANDA	ANDA202261	Aurobindo Pharma Limited	MINOCYCLINE HYDROCHLORIDE	45 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-554-99)
65862-884-05	65862-884	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160613	N/A	ANDA	ANDA202261	Aurobindo Pharma Limited	MINOCYCLINE HYDROCHLORIDE	80 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-884-05)
65862-883-01	65862-883	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190821	N/A	ANDA	ANDA202261	Aurobindo Pharma Limited	MINOCYCLINE HYDROCHLORIDE	55 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-01)
65862-883-05	65862-883	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190821	N/A	ANDA	ANDA202261	Aurobindo Pharma Limited	MINOCYCLINE HYDROCHLORIDE	55 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-05)