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
79481-0709-1	79481-0709	HUMAN OTC DRUG	Mucus D	guaifenesin and pseudoephedrine hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20250107	N/A	ANDA	ANDA214407	Meijer, Inc.	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (79481-0709-1) / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
0113-8307-68	0113-8307	HUMAN OTC DRUG	mucus D	guaifenesin and pseudoephedrine hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20251003	N/A	ANDA	ANDA214407	L. Perrigo Company	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	2 BLISTER PACK in 1 CARTON (0113-8307-68) / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
0113-8911-62	0113-8911	HUMAN OTC DRUG	Mucus D	guaifenesin, pseudoephedrine hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20251003	N/A	ANDA	ANDA214407	L. Perrigo Company	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	1200 mg/1; 120 mg/1	4 BLISTER PACK in 1 CARTON (0113-8911-62) / 6 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK