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
55111-638-10	55111-638	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20080123	N/A	ANDA	ANDA065436	Dr. Reddy's Laboratories Limited	MINOCYCLINE HYDROCHLORIDE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (55111-638-10)
55111-639-60	55111-639	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20080123	N/A	ANDA	ANDA065436	Dr. Reddy's Laboratories Limited	MINOCYCLINE HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (55111-639-60)
55111-639-10	55111-639	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20080123	N/A	ANDA	ANDA065436	Dr. Reddy's Laboratories Limited	MINOCYCLINE HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (55111-639-10)
55111-639-50	55111-639	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20080123	N/A	ANDA	ANDA065436	Dr. Reddy's Laboratories Limited	MINOCYCLINE HYDROCHLORIDE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (55111-639-50)
55111-638-01	55111-638	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20080123	N/A	ANDA	ANDA065436	Dr. Reddy's Laboratories Limited	MINOCYCLINE HYDROCHLORIDE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (55111-638-01)
55111-637-10	55111-637	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20080123	N/A	ANDA	ANDA065436	Dr. Reddy's Laboratories Limited	MINOCYCLINE HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (55111-637-10)
55111-637-01	55111-637	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED	ORAL	20080123	N/A	ANDA	ANDA065436	Dr. Reddy's Laboratories Limited	MINOCYCLINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (55111-637-01)