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
63629-9211-1	63629-9211	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220302	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	45 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9211-1)
63629-9212-1	63629-9212	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220302	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	55 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9212-1)
63629-9213-1	63629-9213	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220302	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	65 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9213-1)
63629-9214-1	63629-9214	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220302	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9214-1)
63629-9215-1	63629-9215	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220302	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	90 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9215-1)
71335-2201-1	71335-2201	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230804	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	90 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2201-1)
63629-9210-1	63629-9210	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220302	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	135 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9210-1)
63629-9209-1	63629-9209	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220302	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	115 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9209-1)
63629-9208-1	63629-9208	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220302	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	105 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9208-1)
72162-1852-3	72162-1852	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	90 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1852-3)
72162-1838-3	72162-1838	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191223	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	55 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1838-3)
72162-1839-3	72162-1839	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1839-3)
72162-1840-3	72162-1840	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	105 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1840-3)
72162-1854-3	72162-1854	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	45 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1854-3)
72162-1867-3	72162-1867	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	65 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1867-3)
72162-1868-3	72162-1868	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	115 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1868-3)
72162-1853-3	72162-1853	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	135 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1853-3)
71335-2710-1	71335-2710	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250728	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	90 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2710-1)
71335-2711-1	71335-2711	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250728	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	45 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2711-1)
71335-2904-1	71335-2904	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251107	N/A	ANDA	ANDA204453	Bryant Ranch Prepack	MINOCYCLINE HYDROCHLORIDE	105 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2904-1)