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
57664-854-13	57664-854	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (57664-854-13)
57664-854-18	57664-854	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (57664-854-18)
57664-854-85	57664-854	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	50 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (57664-854-85)
57664-854-88	57664-854	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (57664-854-88)
57664-855-13	57664-855	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	75 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (57664-855-13)
57664-855-18	57664-855	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (57664-855-18)
57664-855-85	57664-855	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	75 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (57664-855-85)
57664-855-88	57664-855	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (57664-855-88)
57664-856-13	57664-856	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (57664-856-13)
57664-856-18	57664-856	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (57664-856-18)
57664-856-85	57664-856	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (57664-856-85)
57664-856-88	57664-856	HUMAN PRESCRIPTION DRUG	Minocycline	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20160129	N/A	ANDA	ANDA090217	Sun Pharmaceutical Industries, Inc.	MINOCYCLINE HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (57664-856-88)