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=ANDA078110"
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
71335-1626-2 71335-1626 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20200608 N/A ANDA ANDA078110 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 2 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1626-2)
71335-1626-3 71335-1626 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20200608 N/A ANDA ANDA078110 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE 2 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1626-3)
43547-271-10 43547-271 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE 2 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-271-10)
43547-271-50 43547-271 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE 2 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-271-50)
43547-595-10 43547-595 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE .25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-595-10)
43547-595-50 43547-595 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE .25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-595-50)
43547-599-10 43547-599 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE 3 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-599-10)
43547-599-50 43547-599 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE 3 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-599-50)
50268-741-15 50268-741 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20220819 N/A ANDA ANDA078110 AvPAK ROPINIROLE HYDROCHLORIDE .25 mg/1 50 BLISTER PACK in 1 BOX (50268-741-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-741-11)
60687-577-01 60687-577 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20210610 N/A ANDA ANDA078110 American Health Packaging ROPINIROLE HYDROCHLORIDE .25 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-577-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-577-11)
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