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
62135-523-90	62135-523	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230411	N/A	ANDA	ANDA077127	Chartwell RX, LLC	NIFEDIPINE	90 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-523-90)
50090-4158-0	50090-4158	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190225	N/A	ANDA	ANDA077127	A-S Medication Solutions	NIFEDIPINE	90 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4158-0)
50090-4158-1	50090-4158	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230414	N/A	ANDA	ANDA077127	A-S Medication Solutions	NIFEDIPINE	90 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4158-1)
55289-798-07	55289-798	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20111021	N/A	ANDA	ANDA077127	PD-Rx Pharmaceuticals, Inc.	NIFEDIPINE	30 mg/1	7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-798-07)
55289-798-30	55289-798	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20111021	N/A	ANDA	ANDA077127	PD-Rx Pharmaceuticals, Inc.	NIFEDIPINE	30 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-798-30)
62135-521-90	62135-521	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230411	N/A	ANDA	ANDA077127	Chartwell RX, LLC	NIFEDIPINE	30 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-521-90)
62175-260-46	62175-260	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20051121	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	30 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-260-46)
62175-261-46	62175-261	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20051121	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	60 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-46)
62175-261-55	62175-261	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20051121	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	60 mg/1	300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-55)
62175-262-32	62175-262	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20071003	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	90 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-32)
62175-262-37	62175-262	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20071003	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	90 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-37)
62175-262-46	62175-262	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20071003	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	90 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-46)
62175-260-55	62175-260	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20051121	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	30 mg/1	300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-260-55)
62175-260-37	62175-260	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20051121	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	30 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-260-37)
62175-261-37	62175-261	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20051121	N/A	ANDA	ANDA077127	Lannett Company, Inc.	NIFEDIPINE	60 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-37)