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
63941-245-02	63941-245	HUMAN OTC DRUG	All Day Pain Relief	NAPROXEN SODIUM	TABLET, COATED	ORAL	20100519	20261130	ANDA	ANDA079096	VALU MERCHANDISERS COMPANY	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (63941-245-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-245-03	63941-245	HUMAN OTC DRUG	All Day Pain Relief	NAPROXEN SODIUM	TABLET, COATED	ORAL	20100519	20270930	ANDA	ANDA079096	VALU MERCHANDISERS COMPANY	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
68998-144-03	68998-144	HUMAN OTC DRUG	Naproxen Sodium	NAPROXEN SODIUM	TABLET, COATED	ORAL	20090601	N/A	ANDA	ANDA079096	Marc Glassman, Inc.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (68998-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
68998-145-03	68998-145	HUMAN OTC DRUG	Naproxen Sodium	NAPROXEN SODIUM	TABLET, COATED	ORAL	20090531	N/A	ANDA	ANDA079096	Marc Glassman, Inc.	NAPROXEN SODIUM	220 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (68998-145-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
85766-121-01	85766-121	HUMAN OTC DRUG	Medique Mediproxen	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20251217	N/A	ANDA	ANDA079096	Sportpharm, Inc. dba Sportpharm	NAPROXEN SODIUM	220 mg/1	1 TABLET, FILM COATED in 1 PACKET (85766-121-01)
85766-121-10	85766-121	HUMAN OTC DRUG	Medique Mediproxen	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20251217	N/A	ANDA	ANDA079096	Sportpharm, Inc. dba Sportpharm	NAPROXEN SODIUM	220 mg/1	100 PACKET in 1 BOX (85766-121-10) / 1 TABLET, FILM COATED in 1 PACKET (85766-121-01)
85766-121-50	85766-121	HUMAN OTC DRUG	Medique Mediproxen	NAPROXEN SODIUM	TABLET, FILM COATED	ORAL	20251217	N/A	ANDA	ANDA079096	Sportpharm, Inc. dba Sportpharm	NAPROXEN SODIUM	220 mg/1	50 PACKET in 1 BOX (85766-121-50) / 1 TABLET, FILM COATED in 1 PACKET