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
61919-324-30	61919-324	HUMAN PRESCRIPTION DRUG	DICYCLOMINE HYDROCHLORIDE	DICYCLOMINE HYDROCHLORIDE	TABLET	ORAL	20150101	N/A	ANDA	ANDA085223	DIRECT RX	DICYCLOMINE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (61919-324-30)
70934-682-30	70934-682	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20200429	20241031	ANDA	ANDA085223	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	DICYCLOMINE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70934-682-30)
70934-757-90	70934-757	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20221012	20250331	ANDA	ANDA085223	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	DICYCLOMINE HYDROCHLORIDE	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70934-757-90)
53002-3450-1	53002-3450	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20181001	N/A	ANDA	ANDA085223	RPK Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	10 TABLET in 1 BOTTLE (53002-3450-1)
53002-3450-2	53002-3450	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20181001	N/A	ANDA	ANDA085223	RPK Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	20 TABLET in 1 BOTTLE (53002-3450-2)
53002-3450-3	53002-3450	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20181001	N/A	ANDA	ANDA085223	RPK Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (53002-3450-3)