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
68382-552-01	68382-552	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	105 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-01)
68382-552-05	68382-552	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	105 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-05)
68382-552-06	68382-552	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	105 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-06)
68382-552-10	68382-552	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	105 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-10)
68382-552-16	68382-552	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	105 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-16)
68382-552-30	68382-552	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	105 mg/1	10 BLISTER PACK in 1 CARTON (68382-552-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1153-0	70771-1153	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	55 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-0)
70771-1153-1	70771-1153	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	55 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-1)
68382-551-05	68382-551	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	80 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-05)
68382-551-06	68382-551	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	80 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-06)
68382-551-10	68382-551	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	80 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-10)
68382-551-16	68382-551	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	80 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-16)
68382-551-30	68382-551	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	80 mg/1	10 BLISTER PACK in 1 CARTON (68382-551-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
68382-551-01	68382-551	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	80 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-551-01)
70771-1156-0	70771-1156	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	90 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1156-0)
70771-1156-1	70771-1156	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	90 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1156-1)
68382-550-01	68382-550	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	55 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-550-01)
68382-550-05	68382-550	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	55 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-550-05)
68382-550-06	68382-550	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	55 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-550-06)
68382-550-10	68382-550	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Pharmaceuticals (USA) Inc.	MINOCYCLINE HYDROCHLORIDE	55 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-550-10)