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=ANDA078578"
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
71335-1985-4 71335-1985 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20211029 N/A ANDA ANDA078578 Bryant Ranch Prepack AMIODARONE HYDROCHLORIDE 200 mg/1 90 TABLET in 1 BOTTLE (71335-1985-4)
71335-1985-5 71335-1985 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20221013 N/A ANDA ANDA078578 Bryant Ranch Prepack AMIODARONE HYDROCHLORIDE 200 mg/1 10 TABLET in 1 BOTTLE (71335-1985-5)
71335-1985-3 71335-1985 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20221013 N/A ANDA ANDA078578 Bryant Ranch Prepack AMIODARONE HYDROCHLORIDE 200 mg/1 60 TABLET in 1 BOTTLE (71335-1985-3)
71335-1985-2 71335-1985 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20221013 N/A ANDA ANDA078578 Bryant Ranch Prepack AMIODARONE HYDROCHLORIDE 200 mg/1 30 TABLET in 1 BOTTLE (71335-1985-2)
71335-1985-1 71335-1985 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20221013 N/A ANDA ANDA078578 Bryant Ranch Prepack AMIODARONE HYDROCHLORIDE 200 mg/1 200 TABLET in 1 BOTTLE (71335-1985-1)
72888-039-05 72888-039 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20200309 N/A ANDA ANDA078578 Advagen Pharma Limited AMIODARONE HYDROCHLORIDE 200 mg/1 500 TABLET in 1 BOTTLE (72888-039-05)
72888-039-09 72888-039 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20200309 N/A ANDA ANDA078578 Advagen Pharma Limited AMIODARONE HYDROCHLORIDE 200 mg/1 10 BLISTER PACK in 1 CARTON (72888-039-09) / 10 TABLET in 1 BLISTER PACK
72888-039-60 72888-039 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20200309 N/A ANDA ANDA078578 Advagen Pharma Limited AMIODARONE HYDROCHLORIDE 200 mg/1 60 TABLET in 1 BOTTLE (72888-039-60)
72888-061-30 72888-061 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20200821 N/A ANDA ANDA078578 Advagen Pharma Limited AMIODARONE HYDROCHLORIDE 400 mg/1 30 TABLET in 1 BOTTLE (72888-061-30)
72888-060-30 72888-060 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20200821 N/A ANDA ANDA078578 Advagen Pharma Limited AMIODARONE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE (72888-060-30)
70518-3439-0 70518-3439 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20220614 N/A ANDA ANDA078578 REMEDYREPACK INC. AMIODARONE HYDROCHLORIDE 200 mg/1 30 TABLET in 1 BLISTER PACK (70518-3439-0)
70518-3439-1 70518-3439 HUMAN PRESCRIPTION DRUG Amiodarone Hydrochloride Amiodarone Hydrochloride TABLET ORAL 20221218 N/A ANDA ANDA078578 REMEDYREPACK INC. AMIODARONE HYDROCHLORIDE 200 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-3439-1)
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