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
0069-2660-41	0069-2660	HUMAN PRESCRIPTION DRUG	Procardia XL	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	19890906	N/A	NDA	NDA019684	Pfizer Laboratories Div Pfizer Inc	NIFEDIPINE	60 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2660-41)
0069-2660-66	0069-2660	HUMAN PRESCRIPTION DRUG	Procardia XL	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	19890906	N/A	NDA	NDA019684	Pfizer Laboratories Div Pfizer Inc	NIFEDIPINE	60 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2660-66)
0069-2660-72	0069-2660	HUMAN PRESCRIPTION DRUG	Procardia XL	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	19890906	N/A	NDA	NDA019684	Pfizer Laboratories Div Pfizer Inc	NIFEDIPINE	60 mg/1	300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2660-72)
0069-2670-66	0069-2670	HUMAN PRESCRIPTION DRUG	Procardia XL	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	19890906	N/A	NDA	NDA019684	Pfizer Laboratories Div Pfizer Inc	NIFEDIPINE	90 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2670-66)
0069-2650-72	0069-2650	HUMAN PRESCRIPTION DRUG	Procardia XL	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	19890906	N/A	NDA	NDA019684	Pfizer Laboratories Div Pfizer Inc	NIFEDIPINE	30 mg/1	300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-72)
0069-2650-66	0069-2650	HUMAN PRESCRIPTION DRUG	Procardia XL	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	19890906	N/A	NDA	NDA019684	Pfizer Laboratories Div Pfizer Inc	NIFEDIPINE	30 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-66)
0069-2650-41	0069-2650	HUMAN PRESCRIPTION DRUG	Procardia XL	nifedipine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	19890906	N/A	NDA	NDA019684	Pfizer Laboratories Div Pfizer Inc	NIFEDIPINE	30 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2650-41)