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
30142-739-68	30142-739	HUMAN OTC DRUG	mucus d	guaifenesin and pseudoephedrine hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20251104	N/A	ANDA	ANDA214407	Kroger Company	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	2 BLISTER PACK in 1 CARTON (30142-739-68) / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
51316-878-68	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	2 BLISTER PACK in 1 CARTON (51316-878-68) / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
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