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
51316-878-89	51316-878	HUMAN OTC DRUG	MUCUS D	guaifenesin and pseudoephedrine hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20250404	N/A	ANDA	ANDA214407	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (51316-878-89) / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
0363-8708-68	0363-8708	HUMAN OTC DRUG	Mucus Relief D	guaifenesin and pseudoephedrine hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20240326	N/A	ANDA	ANDA214407	Walgreen Company	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	2 BLISTER PACK in 1 CARTON (0363-8708-68) / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
79903-388-24	79903-388	HUMAN OTC DRUG	EQUATE MUCUS D	guaifenesin, pseudoephedrine hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20251205	N/A	ANDA	ANDA214407	WALMART INC.	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	1200 mg/1; 120 mg/1	4 BLISTER PACK in 1 CARTON (79903-388-24) / 6 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK