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
68788-7642-9	68788-7642	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20200228	N/A	ANDA	ANDA210614	Preferred Pharmaceuticals, Inc.	NIFEDIPINE	30 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-9)
50742-260-01	50742-260	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190312	N/A	ANDA	ANDA210614	Ingenus Pharmaceuticals, LLC	NIFEDIPINE	30 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-260-01)
0904-7081-06	0904-7081	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20190312	N/A	ANDA	ANDA210614	Major Pharmaceuticals	NIFEDIPINE	60 mg/1	50 BLISTER PACK in 1 CARTON (0904-7081-06) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0904-7081-61	0904-7081	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20190312	N/A	ANDA	ANDA210614	Major Pharmaceuticals	NIFEDIPINE	60 mg/1	100 BLISTER PACK in 1 CARTON (0904-7081-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70518-2679-0	70518-2679	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20200408	N/A	ANDA	ANDA210614	REMEDYREPACK INC.	NIFEDIPINE	30 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2679-0)
60760-859-90	60760-859	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20240601	N/A	ANDA	ANDA210614	ST. MARY'S MEDICAL PARK PHARMACY	NIFEDIPINE	60 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-859-90)
50742-260-03	50742-260	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190312	N/A	ANDA	ANDA210614	Ingenus Pharmaceuticals, LLC	NIFEDIPINE	30 mg/1	300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-260-03)
50742-260-30	50742-260	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190312	N/A	ANDA	ANDA210614	Ingenus Pharmaceuticals, LLC	NIFEDIPINE	30 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-260-30)
50742-261-30	50742-261	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190312	N/A	ANDA	ANDA210614	Ingenus Pharmaceuticals, LLC	NIFEDIPINE	60 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50742-261-30)
60760-862-90	60760-862	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20240604	N/A	ANDA	ANDA210614	ST. MARY'S MEDICAL PARK PHARMACY	NIFEDIPINE	90 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-862-90)
0904-7082-04	0904-7082	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20190312	N/A	ANDA	ANDA210614	Major Pharmaceuticals	NIFEDIPINE	90 mg/1	30 BLISTER PACK in 1 CARTON (0904-7082-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0904-7082-06	0904-7082	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20190312	N/A	ANDA	ANDA210614	Major Pharmaceuticals	NIFEDIPINE	90 mg/1	50 BLISTER PACK in 1 CARTON (0904-7082-06) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
50090-6201-0	50090-6201	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20221102	N/A	ANDA	ANDA210614	A-S Medication Solutions	NIFEDIPINE	60 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6201-0)
50090-6201-2	50090-6201	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20221102	N/A	ANDA	ANDA210614	A-S Medication Solutions	NIFEDIPINE	60 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6201-2)
0615-8549-39	0615-8549	HUMAN PRESCRIPTION DRUG	Nifedipine	nifedipine	TABLET, EXTENDED RELEASE	ORAL	20241010	N/A	ANDA	ANDA210614	NCS HealthCare of KY, LLC dba Vangard Labs	NIFEDIPINE	60 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8549-39)