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)
42291-523-10	42291-523	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20170731	N/A	ANDA	ANDA078703	AvKARE	PROPRANOLOL HYDROCHLORIDE	80 mg/1	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-10)
63629-9282-1	63629-9282	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220606	N/A	ANDA	ANDA078703	Bryant Ranch Prepack	PROPRANOLOL HYDROCHLORIDE	120 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-9282-1)
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)
60687-215-01	60687-215	HUMAN PRESCRIPTION DRUG	Propranolol Hydrochloride	Propranolol Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20170301	N/A	ANDA	ANDA078703	American Health Packaging	PROPRANOLOL HYDROCHLORIDE	60 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-215-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-215-11)
72162-1604-1	72162-1604	HUMAN PRESCRIPTION DRUG	propranolol hydrochloride	propranolol hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20130311	N/A	ANDA	ANDA078703	Bryant Ranch Prepack	PROPRANOLOL HYDROCHLORIDE	120 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1604-1)