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
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)
70771-1153-3	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	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-3)
70771-1153-5	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	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-5)
70771-1153-7	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	10 BLISTER PACK in 1 CARTON (70771-1153-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1153-9	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	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-9)
70771-1157-0	70771-1157	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	105 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-0)
70771-1157-1	70771-1157	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	105 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-1)
70771-1154-0	70771-1154	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	65 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-0)
70771-1154-1	70771-1154	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	65 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-1)
70771-1154-3	70771-1154	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	65 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-3)
70771-1154-5	70771-1154	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	65 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-5)
70771-1154-7	70771-1154	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	65 mg/1	10 BLISTER PACK in 1 CARTON (70771-1154-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70771-1154-9	70771-1154	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	65 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1154-9)
70771-1158-0	70771-1158	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	115 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1158-0)
70771-1158-1	70771-1158	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20250612	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	115 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1158-1)
70771-1155-0	70771-1155	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	80 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1155-0)
70771-1155-1	70771-1155	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	80 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1155-1)
70771-1155-3	70771-1155	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	80 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1155-3)
70771-1155-5	70771-1155	HUMAN PRESCRIPTION DRUG	minocycline hydrochloride	minocycline hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180307	N/A	ANDA	ANDA203553	Zydus Lifesciences Limited	MINOCYCLINE HYDROCHLORIDE	80 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1155-5)