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	上市日期	结束日期	市场类别	申请号	标签持有者	包装描述
51862-896-01	51862-896	HUMAN PRESCRIPTION DRUG	Tilia Fe	NdAc and EE Tablets and Ferrous Fumarate Tablets	KIT	20201015	N/A	ANDA	ANDA202962	Mayne Pharma Inc.	1 BLISTER PACK in 1 PACKET (51862-896-01) / 1 KIT in 1 BLISTER PACK
51862-896-02	51862-896	HUMAN PRESCRIPTION DRUG	Tilia Fe	NdAc and EE Tablets and Ferrous Fumarate Tablets	KIT	20201015	N/A	ANDA	ANDA202962	Mayne Pharma Inc.	1 BLISTER PACK in 1 CARTON (51862-896-02) / 1 KIT in 1 BLISTER PACK
51862-896-03	51862-896	HUMAN PRESCRIPTION DRUG	Tilia Fe	NdAc and EE Tablets and Ferrous Fumarate Tablets	KIT	20201015	N/A	ANDA	ANDA202962	Mayne Pharma Inc.	3 BLISTER PACK in 1 CARTON (51862-896-03) / 1 KIT in 1 BLISTER PACK
51862-896-06	51862-896	HUMAN PRESCRIPTION DRUG	Tilia Fe	NdAc and EE Tablets and Ferrous Fumarate Tablets	KIT	20201015	N/A	ANDA	ANDA202962	Mayne Pharma Inc.	6 BLISTER PACK in 1 CARTON (51862-896-06) / 1 KIT in 1 BLISTER PACK
75907-086-28	75907-086	HUMAN PRESCRIPTION DRUG	Tilia Fe	NdAc and EE Tablets and Ferrous Fumarate Tablets	KIT	20240601	N/A	ANDA	ANDA202962	Dr. Reddy’s Laboratories Inc.	1 BLISTER PACK in 1 PACKET (75907-086-28) / 1 KIT in 1 BLISTER PACK
75907-086-32	75907-086	HUMAN PRESCRIPTION DRUG	Tilia Fe	NdAc and EE Tablets and Ferrous Fumarate Tablets	KIT	20240601	N/A	ANDA	ANDA202962	Dr. Reddy’s Laboratories Inc.	3 BLISTER PACK in 1 CARTON (75907-086-32) / 1 KIT in 1 BLISTER PACK