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
62332-110-31 62332-110 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 8 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-110-31)
62332-110-71 62332-110 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 8 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-110-71)
62332-110-90 62332-110 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 8 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-110-90)
62332-110-91 62332-110 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20200620 N/A ANDA ANDA202786 Alembic Pharmaceuticals Inc. ROPINIROLE HYDROCHLORIDE 8 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-110-91)
62332-111-10 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/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (62332-111-10)
62332-111-30 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 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-111-30)
62332-111-31 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/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-111-31)
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)
46708-262-10 46708-262 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 2 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-262-10)
46708-262-30 46708-262 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 2 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-30)
46708-262-31 46708-262 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 2 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-31)
46708-262-71 46708-262 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 2 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-71)
46708-262-90 46708-262 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 2 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-90)
46708-262-91 46708-262 HUMAN PRESCRIPTION DRUG Ropinirole Ropinirole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20130314 N/A ANDA ANDA202786 Alembic Pharmaceuticals Limited ROPINIROLE HYDROCHLORIDE 2 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-262-91)
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)
46708-263-30 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 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-263-30)
46708-263-31 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 BOTTLE (46708-263-31)
46708-263-71 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/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-263-71)
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