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
51655-034-83	51655-034	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230111	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	3.125 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-83)
51655-397-25	51655-397	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-25)
51655-397-26	51655-397	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20200708	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-26)
51655-397-52	51655-397	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-52)
51655-397-83	51655-397	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230310	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-83)
60760-494-60	60760-494	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190604	N/A	ANDA	ANDA077614	St. Mary's Medical Park Pharmacy	CARVEDILOL	12.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-494-60)
60760-582-60	60760-582	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20221017	N/A	ANDA	ANDA077614	ST. MARY'S MEDICAL PARK PHARMACY	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-582-60)
65841-616-01	65841-616	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-616-01)
65841-616-05	65841-616	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-616-05)
65841-616-17	65841-616	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	3.125 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (65841-616-17)
50090-1062-0	50090-1062	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-1062-0)
50090-1062-1	50090-1062	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	3.125 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (50090-1062-1)
50090-1062-2	50090-1062	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	3.125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-1062-2)
65841-617-01	65841-617	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-617-01)
65841-618-05	65841-618	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-618-05)
65841-618-17	65841-618	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	12.5 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (65841-618-17)
65841-619-01	65841-619	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-619-01)
65841-619-05	65841-619	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-619-05)
65841-619-17	65841-619	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	25 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (65841-619-17)
68071-2230-3	68071-2230	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20250102	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	12.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-3)