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
71335-0736-4	71335-0736	HUMAN PRESCRIPTION DRUG	Morphine sulfate	morphine sulfate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA078761	Bryant Ranch Prepack	MORPHINE SULFATE	15 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-4)
71335-0736-5	71335-0736	HUMAN PRESCRIPTION DRUG	Morphine sulfate	morphine sulfate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA078761	Bryant Ranch Prepack	MORPHINE SULFATE	15 mg/1	40 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-5)
71335-0736-6	71335-0736	HUMAN PRESCRIPTION DRUG	Morphine sulfate	morphine sulfate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA078761	Bryant Ranch Prepack	MORPHINE SULFATE	15 mg/1	14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-6)
71335-0736-7	71335-0736	HUMAN PRESCRIPTION DRUG	Morphine sulfate	morphine sulfate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA078761	Bryant Ranch Prepack	MORPHINE SULFATE	15 mg/1	15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-7)
71335-0736-8	71335-0736	HUMAN PRESCRIPTION DRUG	Morphine sulfate	morphine sulfate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA078761	Bryant Ranch Prepack	MORPHINE SULFATE	15 mg/1	20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-8)
71335-0736-9	71335-0736	HUMAN PRESCRIPTION DRUG	Morphine sulfate	morphine sulfate	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA078761	Bryant Ranch Prepack	MORPHINE SULFATE	15 mg/1	84 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-9)