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
51991-820-01	51991-820	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20130311	N/A	ANDA	ANDA078703	Breckenridge Pharmaceutical, Inc.	PROPRANOLOL HYDROCHLORIDE	160 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-01)
51991-820-05	51991-820	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20130311	N/A	ANDA	ANDA078703	Breckenridge Pharmaceutical, Inc.	PROPRANOLOL HYDROCHLORIDE	160 mg/1	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-05)
72162-1602-1	72162-1602	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20130311	N/A	ANDA	ANDA078703	Bryant Ranch Prepack	PROPRANOLOL HYDROCHLORIDE	60 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1602-1)
70518-1463-0	70518-1463	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20181004	N/A	ANDA	ANDA078703	REMEDYREPACK INC.	PROPRANOLOL HYDROCHLORIDE	120 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1463-0)
51991-818-01	51991-818	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20130311	N/A	ANDA	ANDA078703	Breckenridge Pharmaceutical, Inc.	PROPRANOLOL HYDROCHLORIDE	80 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-818-01)
51991-818-05	51991-818	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20130311	N/A	ANDA	ANDA078703	Breckenridge Pharmaceutical, Inc.	PROPRANOLOL HYDROCHLORIDE	80 mg/1	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-818-05)