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
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)
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)
62332-110-10	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 CARTON (62332-110-10)
62332-110-30	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	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-110-30)
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)