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
51407-875-30	51407-875	HUMAN PRESCRIPTION DRUG	Amiodarone Hydrochloride	Amiodarone Hydrochloride	TABLET	ORAL	20240115	N/A	ANDA	ANDA076362	Golden State Medical Supply, Inc.	AMIODARONE HYDROCHLORIDE	400 mg/1	30 TABLET in 1 BOTTLE (51407-875-30)
51672-4056-0	51672-4056	HUMAN PRESCRIPTION DRUG	Amiodarone Hydrochloride	Amiodarone Hydrochloride	TABLET	ORAL	20031202	N/A	ANDA	ANDA076362	Taro Pharmaceuticals U.S.A., Inc.	AMIODARONE HYDROCHLORIDE	300 mg/1	10 BLISTER PACK in 1 CARTON (51672-4056-0) / 10 TABLET in 1 BLISTER PACK
51672-4056-1	51672-4056	HUMAN PRESCRIPTION DRUG	Amiodarone Hydrochloride	Amiodarone Hydrochloride	TABLET	ORAL	20031202	N/A	ANDA	ANDA076362	Taro Pharmaceuticals U.S.A., Inc.	AMIODARONE HYDROCHLORIDE	300 mg/1	100 TABLET in 1 BOTTLE (51672-4056-1)
51672-4056-3	51672-4056	HUMAN PRESCRIPTION DRUG	Amiodarone Hydrochloride	Amiodarone Hydrochloride	TABLET	ORAL	20031202	N/A	ANDA	ANDA076362	Taro Pharmaceuticals U.S.A., Inc.	AMIODARONE HYDROCHLORIDE	300 mg/1	1000 TABLET in 1 BOTTLE (51672-4056-3)
51672-4056-6	51672-4056	HUMAN PRESCRIPTION DRUG	Amiodarone Hydrochloride	Amiodarone Hydrochloride	TABLET	ORAL	20031202	N/A	ANDA	ANDA076362	Taro Pharmaceuticals U.S.A., Inc.	AMIODARONE HYDROCHLORIDE	300 mg/1	30 TABLET in 1 BOTTLE (51672-4056-6)
51672-4057-0	51672-4057	HUMAN PRESCRIPTION DRUG	Amiodarone Hydrochloride	Amiodarone Hydrochloride	TABLET	ORAL	20021129	N/A	ANDA	ANDA076362	Taro Pharmaceuticals U.S.A., Inc.	AMIODARONE HYDROCHLORIDE	400 mg/1	10 BLISTER PACK in 1 CARTON (51672-4057-0) / 10 TABLET in 1 BLISTER PACK
51672-4057-6	51672-4057	HUMAN PRESCRIPTION DRUG	Amiodarone Hydrochloride	Amiodarone Hydrochloride	TABLET	ORAL	20021129	N/A	ANDA	ANDA076362	Taro Pharmaceuticals U.S.A., Inc.	AMIODARONE HYDROCHLORIDE	400 mg/1	30 TABLET in 1 BOTTLE (51672-4057-6)