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
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)
43547-596-10 43547-596 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE .5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-596-10)
43547-596-50 43547-596 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE .5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-596-50)
43547-600-10 43547-600 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE 4 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-600-10)
43547-600-50 43547-600 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-600-50)
71335-1626-1 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 30 TABLET, FILM COATED in 1 BOTTLE (71335-1626-1)
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)
50268-743-15 50268-743 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20220819 N/A ANDA ANDA078110 AvPAK ROPINIROLE HYDROCHLORIDE 1 mg/1 50 BLISTER PACK in 1 BOX (50268-743-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-743-11)
71335-0587-1 71335-0587 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20161209 N/A ANDA ANDA078110 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE .25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0587-1)
71335-0587-2 71335-0587 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20161209 N/A ANDA ANDA078110 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE .25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0587-2)
71335-0587-3 71335-0587 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20161209 N/A ANDA ANDA078110 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE .25 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (71335-0587-3)
71335-0587-4 71335-0587 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20161209 N/A ANDA ANDA078110 Bryant Ranch Prepack ROPINIROLE HYDROCHLORIDE .25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-0587-4)
51655-360-26 51655-360 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20200528 N/A ANDA ANDA078110 Northwind Pharmaceuticals, LLC ROPINIROLE HYDROCHLORIDE .25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-360-26)
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)
50268-744-15 50268-744 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20220819 N/A ANDA ANDA078110 AvPAK ROPINIROLE HYDROCHLORIDE 2 mg/1 50 BLISTER PACK in 1 BOX (50268-744-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-744-11)
60687-588-01 60687-588 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20210609 N/A ANDA ANDA078110 American Health Packaging ROPINIROLE HYDROCHLORIDE 1 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-588-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-588-11)
43547-269-10 43547-269 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE .5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-269-10)
43547-269-50 43547-269 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE .5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-269-50)
43547-273-10 43547-273 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE 4 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-273-10)
43547-273-50 43547-273 HUMAN PRESCRIPTION DRUG ropinirole hydrochloride ropinirole hydrochloride TABLET, FILM COATED ORAL 20110920 N/A ANDA ANDA078110 SOLCO HEALTHCARE US, LLC ROPINIROLE HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-273-50)
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