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
59726-915-90	59726-915	HUMAN OTC DRUG	All Day Allergy Relief	Loratadine	TABLET	ORAL	20191030	N/A	ANDA	ANDA075209	P & L Development, LLC	LORATADINE	10 mg/1	1 BOTTLE, PLASTIC in 1 BOX (59726-915-90) / 90 TABLET in 1 BOTTLE, PLASTIC
54473-166-32	54473-166	HUMAN OTC DRUG	CounterAct Allergy	Loratadine	TABLET	ORAL	20250228	N/A	ANDA	ANDA075209	Melaleuca, Inc.	LORATADINE	10 mg/1	1 BOTTLE in 1 BOX (54473-166-32) / 30 TABLET in 1 BOTTLE
63868-577-01	63868-577	HUMAN OTC DRUG	Allergy Relief	Loratadine	TABLET	ORAL	20191227	20251227	ANDA	ANDA075209	QUALITY CHOICE (Chain Drug Marketing Association)	LORATADINE	10 mg/1	1 BOTTLE, PLASTIC in 1 BOX (63868-577-01) / 100 TABLET in 1 BOTTLE, PLASTIC
63868-577-10	63868-577	HUMAN OTC DRUG	Allergy Relief	Loratadine	TABLET	ORAL	20191227	20251227	ANDA	ANDA075209	QUALITY CHOICE (Chain Drug Marketing Association)	LORATADINE	10 mg/1	10 BLISTER PACK in 1 CARTON (63868-577-10) / 1 TABLET in 1 BLISTER PACK
63868-577-30	63868-577	HUMAN OTC DRUG	Allergy Relief	Loratadine	TABLET	ORAL	20191227	20251227	ANDA	ANDA075209	QUALITY CHOICE (Chain Drug Marketing Association)	LORATADINE	10 mg/1	1 BOTTLE, PLASTIC in 1 BOX (63868-577-30) / 30 TABLET in 1 BOTTLE, PLASTIC
83324-150-01	83324-150	HUMAN OTC DRUG	Allergy Relief	Loratadine	TABLET	ORAL	20240731	N/A	ANDA	ANDA075209	QUALITY CHOICE (Chain Drug Marketing Association)	LORATADINE	10 mg/1	1 BOTTLE, PLASTIC in 1 BOX (83324-150-01) / 100 TABLET in 1 BOTTLE, PLASTIC