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
63629-9212-1	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)
72789-525-30	72789-525	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250910	N/A	ANDA	ANDA204453	PD-Rx Pharmaceuticals, Inc.	MINOCYCLINE HYDROCHLORIDE	90 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-525-30)
72789-529-30	72789-529	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250910	N/A	ANDA	ANDA204453	PD-Rx Pharmaceuticals, Inc.	MINOCYCLINE HYDROCHLORIDE	115 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-529-30)
67877-438-14	67877-438	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Ascend Laboratories, LLC	MINOCYCLINE HYDROCHLORIDE	105 mg/1	10 BLISTER PACK in 1 CARTON (67877-438-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-438-30	67877-438	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Ascend Laboratories, LLC	MINOCYCLINE HYDROCHLORIDE	105 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-438-30)
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)
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)
63629-9213-1	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)
72789-526-30	72789-526	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250910	N/A	ANDA	ANDA204453	PD-Rx Pharmaceuticals, Inc.	MINOCYCLINE HYDROCHLORIDE	55 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-526-30)
72789-530-30	72789-530	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250910	N/A	ANDA	ANDA204453	PD-Rx Pharmaceuticals, Inc.	MINOCYCLINE HYDROCHLORIDE	135 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-530-30)
67877-436-30	67877-436	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191223	N/A	ANDA	ANDA204453	Ascend Laboratories, LLC	MINOCYCLINE HYDROCHLORIDE	55 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-30)
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)
67877-644-01	67877-644	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Ascend Laboratories, LLC	MINOCYCLINE HYDROCHLORIDE	115 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-01)
67877-644-05	67877-644	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Ascend Laboratories, LLC	MINOCYCLINE HYDROCHLORIDE	115 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-05)
67877-644-14	67877-644	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Ascend Laboratories, LLC	MINOCYCLINE HYDROCHLORIDE	115 mg/1	10 BLISTER PACK in 1 CARTON (67877-644-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-644-30	67877-644	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20160930	N/A	ANDA	ANDA204453	Ascend Laboratories, LLC	MINOCYCLINE HYDROCHLORIDE	115 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-30)
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)
63629-9215-1	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)
72789-524-30	72789-524	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250910	N/A	ANDA	ANDA204453	PD-Rx Pharmaceuticals, Inc.	MINOCYCLINE HYDROCHLORIDE	65 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-524-30)
72789-528-30	72789-528	HUMAN PRESCRIPTION DRUG	Minocycline Hydrochloride	Minocycline Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250910	N/A	ANDA	ANDA204453	PD-Rx Pharmaceuticals, Inc.	MINOCYCLINE HYDROCHLORIDE	105 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-528-30)