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=ANDA078888"
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
71335-2237-5 71335-2237 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20240403 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 7.5 mg/1 60 TABLET in 1 BOTTLE (71335-2237-5)
71335-2237-6 71335-2237 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20240403 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 7.5 mg/1 120 TABLET in 1 BOTTLE (71335-2237-6)
71335-2237-2 71335-2237 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230829 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 7.5 mg/1 90 TABLET in 1 BOTTLE (71335-2237-2)
71335-2237-3 71335-2237 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20240403 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 7.5 mg/1 18 TABLET in 1 BOTTLE (71335-2237-3)
71335-2237-4 71335-2237 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20240403 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 7.5 mg/1 28 TABLET in 1 BOTTLE (71335-2237-4)
50268-135-15 50268-135 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20201021 N/A ANDA ANDA078888 AvPAK BUSPIRONE HYDROCHLORIDE 15 mg/1 50 BLISTER PACK in 1 BOX (50268-135-15) / 1 TABLET in 1 BLISTER PACK (50268-135-11)
68382-623-30 68382-623 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230321 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 7.5 mg/1 100 BLISTER PACK in 1 CARTON (68382-623-30) / 10 TABLET in 1 BLISTER PACK
68382-623-01 68382-623 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230321 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 7.5 mg/1 100 TABLET in 1 BOTTLE (68382-623-01)
68382-623-05 68382-623 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230321 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 7.5 mg/1 500 TABLET in 1 BOTTLE (68382-623-05)
68382-623-10 68382-623 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230321 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 7.5 mg/1 1000 TABLET in 1 BOTTLE (68382-623-10)
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