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
16571-743-03	16571-743	HUMAN PRESCRIPTION DRUG	Glycopyrrolate	Glycopyrrolate	TABLET	ORAL	20201006	N/A	NDA AUTHORIZED GENERIC	NDA012827	Rising Pharma Holdings, Inc.	GLYCOPYRROLATE	1 mg/1	30 TABLET in 1 CONTAINER (16571-743-03)
16571-743-09	16571-743	HUMAN PRESCRIPTION DRUG	Glycopyrrolate	Glycopyrrolate	TABLET	ORAL	20201006	N/A	NDA AUTHORIZED GENERIC	NDA012827	Rising Pharma Holdings, Inc.	GLYCOPYRROLATE	1 mg/1	90 TABLET in 1 CONTAINER (16571-743-09)
16571-744-03	16571-744	HUMAN PRESCRIPTION DRUG	Glycopyrrolate	Glycopyrrolate	TABLET	ORAL	20201006	N/A	NDA AUTHORIZED GENERIC	NDA012827	Rising Pharma Holdings, Inc.	GLYCOPYRROLATE	2 mg/1	30 TABLET in 1 CONTAINER (16571-744-03)
16571-744-09	16571-744	HUMAN PRESCRIPTION DRUG	Glycopyrrolate	Glycopyrrolate	TABLET	ORAL	20201006	N/A	NDA AUTHORIZED GENERIC	NDA012827	Rising Pharma Holdings, Inc.	GLYCOPYRROLATE	2 mg/1	90 TABLET in 1 CONTAINER (16571-744-09)