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
11822-0046-2	11822-0046	HUMAN OTC DRUG	Guaifenesin and Pseudoephedrine HCl	Guaifenesin and Pseudoephedrine HCL	TABLET, EXTENDED RELEASE	ORAL	20220201	N/A	ANDA	ANDA208369	Rite Aid Corporation	GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE	600 mg/1; 60 mg/1	2 BLISTER PACK in 1 CARTON (11822-0046-2) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
55111-799-04	55111-799	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	1200 mg/1; 120 mg/1	4 BLISTER PACK in 1 CARTON (55111-799-04) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-799-06)
55111-799-12	55111-799	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	1200 mg/1; 120 mg/1	1 BLISTER PACK in 1 CARTON (55111-799-12) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
55111-799-24	55111-799	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	1200 mg/1; 120 mg/1	2 BLISTER PACK in 1 CARTON (55111-799-24) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
55111-799-36	55111-799	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	1200 mg/1; 120 mg/1	3 BLISTER PACK in 1 CARTON (55111-799-36) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK