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
55111-798-18	55111-798	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCL	Guaifenesin and Pseudoephedrine HCL	TABLET, EXTENDED RELEASE	ORAL	20171229	N/A	ANDA	ANDA208369	Dr. Reddys Laboratories Limited	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	2 BLISTER PACK in 1 CARTON (55111-798-18) / 9 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
55111-798-35	55111-798	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCL	Guaifenesin and Pseudoephedrine HCL	TABLET, EXTENDED RELEASE	ORAL	20200123	N/A	ANDA	ANDA208369	Dr. Reddys Laboratories Limited	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (55111-798-35) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
55111-798-09	55111-798	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCL	Guaifenesin and Pseudoephedrine HCL	TABLET, EXTENDED RELEASE	ORAL	20171229	N/A	ANDA	ANDA208369	Dr. Reddys Laboratories Limited	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (55111-798-09) / 9 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70677-1011-1	70677-1011	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCL	TABLET, EXTENDED RELEASE	ORAL	20230505	N/A	ANDA	ANDA208369	Strategic Sourcing Services, LLC	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	1 BLISTER PACK in 1 CARTON (70677-1011-1) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
49035-261-12	49035-261	HUMAN OTC DRUG	Mucus Relief D	Guaifenesin and Pseudoephedrine HCL	TABLET, EXTENDED RELEASE	ORAL	20200403	N/A	ANDA	ANDA208369	Wal-mart Stores, Inc.	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	1200 mg/1; 120 mg/1	2 BLISTER PACK in 1 CARTON (49035-261-12) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK