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=ANDA076362"
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
51672-4056-0 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)
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)
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