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）

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
64850-250-30	64850-250	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, EXTENDED RELEASE	ORAL	20251110	N/A	ANDA	ANDA217862	Elite Laboratories, Inc.	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-250-30)
64850-254-30	64850-254	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, EXTENDED RELEASE	ORAL	20251110	N/A	ANDA	ANDA217862	Elite Laboratories, Inc.	ROPINIROLE HYDROCHLORIDE	12 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-254-30)
64850-253-30	64850-253	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, EXTENDED RELEASE	ORAL	20251110	N/A	ANDA	ANDA217862	Elite Laboratories, Inc.	ROPINIROLE HYDROCHLORIDE	8 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-253-30)
64850-252-30	64850-252	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, EXTENDED RELEASE	ORAL	20251110	N/A	ANDA	ANDA217862	Elite Laboratories, Inc.	ROPINIROLE HYDROCHLORIDE	6 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-252-30)
64850-251-30	64850-251	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, EXTENDED RELEASE	ORAL	20251110	N/A	ANDA	ANDA217862	Elite Laboratories, Inc.	ROPINIROLE HYDROCHLORIDE	4 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-251-30)