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=ANDA070979"
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
0121-0908-40 0121-0908 HUMAN PRESCRIPTION DRUG Propranolol Hydrochloride Propranolol Hydrochloride SOLUTION ORAL 20210903 N/A ANDA ANDA070979 Pharmaceutical Associates, Inc. PROPRANOLOL HYDROCHLORIDE 20 mg/5mL 4 TRAY in 1 CASE (0121-0908-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0908-05)
17856-8728-1 17856-8728 HUMAN PRESCRIPTION DRUG Propranolol Hydrochloride Propranolol Hydrochloride SOLUTION ORAL 20251001 N/A ANDA ANDA070979 ATLANTIC BIOLOGICALS CORP. PROPRANOLOL HYDROCHLORIDE 20 mg/5mL 50 CUP in 1 CASE (17856-8728-1) / 5 mL in 1 CUP
17856-3728-1 17856-3728 HUMAN PRESCRIPTION DRUG Propranolol Hydrochloride Propranolol Hydrochloride SOLUTION ORAL 20240510 N/A ANDA ANDA070979 ATLANTIC BIOLOGICALS CORP. PROPRANOLOL HYDROCHLORIDE 20 mg/5mL 72 CUP in 1 CASE (17856-3728-1) / 5 mL in 1 CUP
0054-3727-63 0054-3727 HUMAN PRESCRIPTION DRUG Propranolol Hydrochloride Propranolol Hydrochloride SOLUTION ORAL 19870515 N/A ANDA ANDA070979 Hikma Pharmaceuticals USA Inc. PROPRANOLOL HYDROCHLORIDE 20 mg/5mL 500 mL in 1 BOTTLE, PLASTIC (0054-3727-63)
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