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
72162-2200-1	72162-2200	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20231215	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2200-1)
70518-4318-0	70518-4318	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20250325	N/A	ANDA	ANDA079229	REMEDYREPACK INC.	ROPINIROLE HYDROCHLORIDE	.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4318-0)
71335-2515-2	71335-2515	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20241024	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-2)
71335-2515-1	71335-2515	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20241024	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-1)
71335-2515-3	71335-2515	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20241024	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	2 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-3)
69452-358-20	69452-358	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA079229	Bionpharma Inc.	ROPINIROLE HYDROCHLORIDE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-358-20)
69452-361-20	69452-361	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA079229	Bionpharma Inc.	ROPINIROLE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-361-20)
69452-362-20	69452-362	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA079229	Bionpharma Inc.	ROPINIROLE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-362-20)
69452-359-20	69452-359	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA079229	Bionpharma Inc.	ROPINIROLE HYDROCHLORIDE	2 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-359-20)
69452-360-20	69452-360	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA079229	Bionpharma Inc.	ROPINIROLE HYDROCHLORIDE	3 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-360-20)
50090-7445-0	50090-7445	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20241106	N/A	ANDA	ANDA079229	A-S Medication Solutions	ROPINIROLE HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7445-0)
71335-2793-1	71335-2793	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260311	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2793-1)
71335-2793-2	71335-2793	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260311	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2793-2)
71335-2793-3	71335-2793	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260311	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.25 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-2793-3)
71335-2793-4	71335-2793	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260311	N/A	ANDA	ANDA079229	Bryant Ranch Prepack	ROPINIROLE HYDROCHLORIDE	.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2793-4)
87063-199-01	87063-199	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260507	N/A	ANDA	ANDA079229	ASCLEMED USA INC.	ROPINIROLE HYDROCHLORIDE	.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-199-01)
87063-200-01	87063-200	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260507	N/A	ANDA	ANDA079229	ASCLEMED USA INC.	ROPINIROLE HYDROCHLORIDE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-200-01)
87063-200-30	87063-200	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260507	N/A	ANDA	ANDA079229	ASCLEMED USA INC.	ROPINIROLE HYDROCHLORIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-200-30)
87063-200-60	87063-200	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260507	N/A	ANDA	ANDA079229	ASCLEMED USA INC.	ROPINIROLE HYDROCHLORIDE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-200-60)
87063-200-90	87063-200	HUMAN PRESCRIPTION DRUG	Ropinirole	Ropinirole	TABLET, FILM COATED	ORAL	20260507	N/A	ANDA	ANDA079229	ASCLEMED USA INC.	ROPINIROLE HYDROCHLORIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-200-90)