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
51655-959-52	51655-959	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230131	N/A	ANDA	ANDA090700	Northwind Pharmaceuticals, LLC	VERAPAMIL HYDROCHLORIDE	180 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-959-52)
68071-3446-0	68071-3446	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230622	N/A	ANDA	ANDA090700	NuCare Pharmaceuticals,Inc.	VERAPAMIL HYDROCHLORIDE	120 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-3446-0)
68788-6328-3	68788-6328	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161017	N/A	ANDA	ANDA090700	Preferred Pharmaceuticals Inc.	VERAPAMIL HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6328-3)
68788-6328-6	68788-6328	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20210928	N/A	ANDA	ANDA090700	Preferred Pharmaceuticals Inc.	VERAPAMIL HYDROCHLORIDE	120 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6328-6)
70518-0605-1	70518-0605	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190731	N/A	ANDA	ANDA090700	REMEDYREPACK INC.	VERAPAMIL HYDROCHLORIDE	180 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0605-1)
72789-416-90	72789-416	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240619	N/A	ANDA	ANDA090700	PD-Rx Pharmaceuticals, Inc.	VERAPAMIL HYDROCHLORIDE	180 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-416-90)
50090-1400-0	50090-1400	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141128	N/A	ANDA	ANDA090700	A-S Medication Solutions	VERAPAMIL HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1400-0)
50090-1400-1	50090-1400	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141128	N/A	ANDA	ANDA090700	A-S Medication Solutions	VERAPAMIL HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1400-1)
63187-849-30	63187-849	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Proficient Rx LP	VERAPAMIL HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-30)
63187-849-60	63187-849	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Proficient Rx LP	VERAPAMIL HYDROCHLORIDE	120 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-60)
63187-849-90	63187-849	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Proficient Rx LP	VERAPAMIL HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-849-90)
68462-292-01	68462-292	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Glenmark Pharmaceuticals Inc., USA	VERAPAMIL HYDROCHLORIDE	120 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-292-01)
68462-292-05	68462-292	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Glenmark Pharmaceuticals Inc., USA	VERAPAMIL HYDROCHLORIDE	120 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-292-05)
68462-292-90	68462-292	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Glenmark Pharmaceuticals Inc., USA	VERAPAMIL HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-292-90)
68462-293-01	68462-293	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Glenmark Pharmaceuticals Inc., USA	VERAPAMIL HYDROCHLORIDE	180 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-293-01)
68462-293-05	68462-293	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Glenmark Pharmaceuticals Inc., USA	VERAPAMIL HYDROCHLORIDE	180 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-293-05)
68462-293-90	68462-293	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20110805	N/A	ANDA	ANDA090700	Glenmark Pharmaceuticals Inc., USA	VERAPAMIL HYDROCHLORIDE	180 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-293-90)
53002-1205-0	53002-1205	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181001	N/A	ANDA	ANDA090700	RPK Pharmaceuticals, Inc.	VERAPAMIL HYDROCHLORIDE	180 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1205-0)
53002-1467-0	53002-1467	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190101	N/A	ANDA	ANDA090700	RPK Pharmaceuticals, Inc.	VERAPAMIL HYDROCHLORIDE	120 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1467-0)
53002-1467-3	53002-1467	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190101	N/A	ANDA	ANDA090700	RPK Pharmaceuticals, Inc.	VERAPAMIL HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1467-3)