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=ANDA070322"
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
68071-2710-3 68071-2710 HUMAN PRESCRIPTION DRUG Propranolol Hydrochloride Propranolol Hydrochloride TABLET ORAL 20220519 N/A ANDA ANDA070322 NuCare Pharmaceuticals,Inc. PROPRANOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (68071-2710-3)
68071-2710-9 68071-2710 HUMAN PRESCRIPTION DRUG Propranolol Hydrochloride Propranolol Hydrochloride TABLET ORAL 20220519 N/A ANDA ANDA070322 NuCare Pharmaceuticals,Inc. PROPRANOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (68071-2710-9)
68788-7791-3 68788-7791 HUMAN PRESCRIPTION DRUG Propranolol Hydrochloride Propranolol Hydrochloride TABLET ORAL 20201021 N/A ANDA ANDA070322 Preferred Pharmaceuticals Inc. PROPRANOLOL HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (68788-7791-3)
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