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=ANDA217862"
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
64850-252-30 64850-252 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20251110 N/A ANDA ANDA217862 Elite Laboratories, Inc. ROPINIROLE HYDROCHLORIDE 6 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-252-30)
72162-2603-3 72162-2603 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 4 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2603-3)
72162-2603-9 72162-2603 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 4 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2603-9)
64850-250-30 64850-250 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20251110 N/A ANDA ANDA217862 Elite Laboratories, Inc. ROPINIROLE HYDROCHLORIDE 2 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-250-30)
64850-254-30 64850-254 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20251110 N/A ANDA ANDA217862 Elite Laboratories, Inc. ROPINIROLE HYDROCHLORIDE 12 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-254-30)
72162-2605-3 72162-2605 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 8 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2605-3)
72162-2605-9 72162-2605 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 8 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2605-9)
64850-251-30 64850-251 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20251110 N/A ANDA ANDA217862 Elite Laboratories, Inc. ROPINIROLE HYDROCHLORIDE 4 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-251-30)
72162-2602-3 72162-2602 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 2 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2602-3)
72162-2602-9 72162-2602 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 2 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2602-9)
72162-2606-3 72162-2606 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 12 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2606-3)
72162-2606-9 72162-2606 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 12 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2606-9)
64850-253-30 64850-253 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20251110 N/A ANDA ANDA217862 Elite Laboratories, Inc. ROPINIROLE HYDROCHLORIDE 8 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-253-30)
72162-2604-3 72162-2604 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 6 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2604-3)
72162-2604-9 72162-2604 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, EXTENDED RELEASE ORAL 20260417 N/A ANDA ANDA217862 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 6 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2604-9)
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