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）
检索条件:" 注册申请号=ANDA079029"
符合检索条件的记录共 15 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
65841-840-06 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)
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)
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)
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)
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
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