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
70518-3693-0	70518-3693	HUMAN PRESCRIPTION DRUG	Dexlansoprazole	Dexlansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20230328	N/A	ANDA	ANDA202294	REMEDYREPACK INC.	DEXLANSOPRAZOLE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3693-0)
72162-2214-3	72162-2214	HUMAN PRESCRIPTION DRUG	Dexlansoprazole	Dexlansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20240105	N/A	ANDA	ANDA202294	Bryant Ranch Prepack	DEXLANSOPRAZOLE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2214-3)
72162-2244-3	72162-2244	HUMAN PRESCRIPTION DRUG	Dexlansoprazole	Dexlansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20240129	N/A	ANDA	ANDA202294	Bryant Ranch Prepack	DEXLANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-2244-3)
49884-147-11	49884-147	HUMAN PRESCRIPTION DRUG	Dexlansoprazole	Dexlansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20230610	N/A	ANDA	ANDA202294	Par Pharmaceutical, Inc.	DEXLANSOPRAZOLE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49884-147-11)
49884-148-09	49884-148	HUMAN PRESCRIPTION DRUG	Dexlansoprazole	Dexlansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20221122	N/A	ANDA	ANDA202294	Par Pharmaceutical, Inc.	DEXLANSOPRAZOLE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49884-148-09)
49884-148-11	49884-148	HUMAN PRESCRIPTION DRUG	Dexlansoprazole	Dexlansoprazole	CAPSULE, DELAYED RELEASE	ORAL	20221122	N/A	ANDA	ANDA202294	Par Pharmaceutical, Inc.	DEXLANSOPRAZOLE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49884-148-11)