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
51672-1317-1	51672-1317	HUMAN PRESCRIPTION DRUG	Betamethasone Dipropionate	Betamethasone Dipropionate	OINTMENT, AUGMENTED	TOPICAL	20041012	N/A	ANDA	ANDA076753	Taro Pharmaceuticals U.S.A., Inc.	BETAMETHASONE DIPROPIONATE	.5 mg/g	1 TUBE in 1 CARTON (51672-1317-1) / 15 g in 1 TUBE
51672-1317-3	51672-1317	HUMAN PRESCRIPTION DRUG	Betamethasone Dipropionate	Betamethasone Dipropionate	OINTMENT, AUGMENTED	TOPICAL	20041012	N/A	ANDA	ANDA076753	Taro Pharmaceuticals U.S.A., Inc.	BETAMETHASONE DIPROPIONATE	.5 mg/g	1 TUBE in 1 CARTON (51672-1317-3) / 50 g in 1 TUBE
51672-1317-5	51672-1317	HUMAN PRESCRIPTION DRUG	Betamethasone Dipropionate	Betamethasone Dipropionate	OINTMENT, AUGMENTED	TOPICAL	20041012	N/A	ANDA	ANDA076753	Taro Pharmaceuticals U.S.A., Inc.	BETAMETHASONE DIPROPIONATE	.5 mg/g	5 g in 1 TUBE (51672-1317-5)