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=ANDA202786"
符合检索条件的记录共 60 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
62332-108-31 62332-108 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 4 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-108-31)
62332-108-71 62332-108 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-108-71)
62332-108-90 62332-108 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 4 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-108-90)
62332-108-91 62332-108 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 4 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-108-91)
46708-264-10 46708-264 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 6 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-264-10)
46708-264-30 46708-264 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 6 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-30)
46708-264-31 46708-264 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 6 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-264-31)
62332-109-10 62332-109 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 6 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (62332-109-10)
62332-109-30 62332-109 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 6 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-109-30)
62332-109-31 62332-109 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 6 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-109-31)
62332-109-71 62332-109 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 6 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-109-71)
62332-109-90 62332-109 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 6 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-109-90)
62332-109-91 62332-109 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 6 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-109-91)
46708-265-10 46708-265 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 8 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-265-10)
46708-265-30 46708-265 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-30)
46708-265-31 46708-265 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 8 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-265-31)
62332-111-71 62332-111 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 12 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-111-71)
62332-111-90 62332-111 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 12 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-111-90)
62332-111-91 62332-111 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 12 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-111-91)
46708-263-10 46708-263 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 4 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-263-10)
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