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
16714-973-01	16714-973	HUMAN PRESCRIPTION DRUG	Phytonadione	Phytonadione	TABLET	ORAL	20220322	N/A	ANDA	ANDA210189	Northstar Rx LLC.	PHYTONADIONE	5 mg/1	1 BOTTLE in 1 CARTON (16714-973-01) / 100 TABLET in 1 BOTTLE
16714-973-02	16714-973	HUMAN PRESCRIPTION DRUG	Phytonadione	Phytonadione	TABLET	ORAL	20220322	N/A	ANDA	ANDA210189	Northstar Rx LLC.	PHYTONADIONE	5 mg/1	1 BOTTLE in 1 CARTON (16714-973-02) / 30 TABLET in 1 BOTTLE
70710-1014-1	70710-1014	HUMAN PRESCRIPTION DRUG	Phytonadione	Phytonadione	TABLET	ORAL	20190222	N/A	ANDA	ANDA210189	Zydus Pharmaceuticals (USA) Inc.	PHYTONADIONE	5 mg/1	1 BOTTLE in 1 CARTON (70710-1014-1) / 100 TABLET in 1 BOTTLE
70710-1014-3	70710-1014	HUMAN PRESCRIPTION DRUG	Phytonadione	Phytonadione	TABLET	ORAL	20211101	N/A	ANDA	ANDA210189	Zydus Pharmaceuticals (USA) Inc.	PHYTONADIONE	5 mg/1	30 TABLET in 1 BOTTLE (70710-1014-3)
70710-1014-4	70710-1014	HUMAN PRESCRIPTION DRUG	Phytonadione	Phytonadione	TABLET	ORAL	20190222	N/A	ANDA	ANDA210189	Zydus Pharmaceuticals (USA) Inc.	PHYTONADIONE	5 mg/1	10 BLISTER PACK in 1 CARTON (70710-1014-4) / 10 TABLET in 1 BLISTER PACK (70710-1014-2)
70771-1318-1	70771-1318	HUMAN PRESCRIPTION DRUG	Phytonadione	Phytonadione	TABLET	ORAL	20190222	N/A	ANDA	ANDA210189	Zydus Lifesciences Limited	PHYTONADIONE	5 mg/1	1 BOTTLE in 1 CARTON (70771-1318-1) / 100 TABLET in 1 BOTTLE
70771-1318-3	70771-1318	HUMAN PRESCRIPTION DRUG	Phytonadione	Phytonadione	TABLET	ORAL	20211101	N/A	ANDA	ANDA210189	Zydus Lifesciences Limited	PHYTONADIONE	5 mg/1	30 TABLET in 1 BOTTLE (70771-1318-3)
70771-1318-4	70771-1318	HUMAN PRESCRIPTION DRUG	Phytonadione	Phytonadione	TABLET	ORAL	20190222	N/A	ANDA	ANDA210189	Zydus Lifesciences Limited	PHYTONADIONE	5 mg/1	10 BLISTER PACK in 1 CARTON (70771-1318-4) / 10 TABLET in 1 BLISTER PACK (70771-1318-2)