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
65841-631-05	65841-631	HUMAN PRESCRIPTION DRUG	Amiodarone hydrochloride	Amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Lifesciences Limited	AMIODARONE HYDROCHLORIDE	200 mg/1	500 TABLET in 1 BOTTLE (65841-631-05)
65841-631-06	65841-631	HUMAN PRESCRIPTION DRUG	Amiodarone hydrochloride	Amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Lifesciences Limited	AMIODARONE HYDROCHLORIDE	200 mg/1	30 TABLET in 1 BOTTLE (65841-631-06)
65841-631-10	65841-631	HUMAN PRESCRIPTION DRUG	Amiodarone hydrochloride	Amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Lifesciences Limited	AMIODARONE HYDROCHLORIDE	200 mg/1	1000 TABLET in 1 BOTTLE (65841-631-10)
65841-631-14	65841-631	HUMAN PRESCRIPTION DRUG	Amiodarone hydrochloride	Amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Lifesciences Limited	AMIODARONE HYDROCHLORIDE	200 mg/1	60 TABLET in 1 BOTTLE (65841-631-14)
65841-631-77	65841-631	HUMAN PRESCRIPTION DRUG	Amiodarone hydrochloride	Amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Lifesciences Limited	AMIODARONE HYDROCHLORIDE	200 mg/1	10 BLISTER PACK in 1 CARTON (65841-631-77) / 10 TABLET in 1 BLISTER PACK
65841-841-06	65841-841	HUMAN PRESCRIPTION DRUG	Amiodarone hydrochloride	Amiodarone hydrochloride	TABLET	ORAL	20230209	N/A	ANDA	ANDA079029	Zydus Lifesciences Limited	AMIODARONE HYDROCHLORIDE	400 mg/1	30 TABLET in 1 BOTTLE (65841-841-06)
63739-051-10	63739-051	HUMAN PRESCRIPTION DRUG	Amiodarone hydrochloride	Amiodarone hydrochloride	TABLET	ORAL	20191206	N/A	ANDA	ANDA079029	McKesson Corporation dba SKY Packaging	AMIODARONE HYDROCHLORIDE	200 mg/1	10 BLISTER PACK in 1 BOX (63739-051-10) / 10 TABLET in 1 BLISTER PACK
65841-840-06	65841-840	HUMAN PRESCRIPTION DRUG	Amiodarone hydrochloride	Amiodarone hydrochloride	TABLET	ORAL	20230209	N/A	ANDA	ANDA079029	Zydus Lifesciences Limited	AMIODARONE HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BOTTLE (65841-840-06)
68382-298-06	68382-298	HUMAN PRESCRIPTION DRUG	amiodarone hydrochloride	amiodarone hydrochloride	TABLET	ORAL	20230209	N/A	ANDA	ANDA079029	Zydus Pharmaceuticals USA Inc.	AMIODARONE HYDROCHLORIDE	400 mg/1	30 TABLET in 1 BOTTLE (68382-298-06)
68382-227-05	68382-227	HUMAN PRESCRIPTION DRUG	amiodarone hydrochloride	amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Pharmaceuticals USA Inc.	AMIODARONE HYDROCHLORIDE	200 mg/1	500 TABLET in 1 BOTTLE (68382-227-05)
68382-227-06	68382-227	HUMAN PRESCRIPTION DRUG	amiodarone hydrochloride	amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Pharmaceuticals USA Inc.	AMIODARONE HYDROCHLORIDE	200 mg/1	30 TABLET in 1 BOTTLE (68382-227-06)
68382-227-10	68382-227	HUMAN PRESCRIPTION DRUG	amiodarone hydrochloride	amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Pharmaceuticals USA Inc.	AMIODARONE HYDROCHLORIDE	200 mg/1	1000 TABLET in 1 BOTTLE (68382-227-10)
68382-227-14	68382-227	HUMAN PRESCRIPTION DRUG	amiodarone hydrochloride	amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Pharmaceuticals USA Inc.	AMIODARONE HYDROCHLORIDE	200 mg/1	60 TABLET in 1 BOTTLE (68382-227-14)
68382-227-77	68382-227	HUMAN PRESCRIPTION DRUG	amiodarone hydrochloride	amiodarone hydrochloride	TABLET	ORAL	20090810	N/A	ANDA	ANDA079029	Zydus Pharmaceuticals USA Inc.	AMIODARONE HYDROCHLORIDE	200 mg/1	100 BLISTER PACK in 1 CARTON (68382-227-77) / 1 TABLET in 1 BLISTER PACK (68382-227-30)
68382-297-06	68382-297	HUMAN PRESCRIPTION DRUG	amiodarone hydrochloride	amiodarone hydrochloride	TABLET	ORAL	20230209	N/A	ANDA	ANDA079029	Zydus Pharmaceuticals USA Inc.	AMIODARONE HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BOTTLE (68382-297-06)