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
68071-3885-2	68071-3885	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20250815	N/A	ANDA	ANDA217566	NuCare Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	20 TABLET in 1 BOTTLE (68071-3885-2)
68071-3885-3	68071-3885	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20250815	N/A	ANDA	ANDA217566	NuCare Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (68071-3885-3)
68071-3885-6	68071-3885	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20251103	N/A	ANDA	ANDA217566	NuCare Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	60 TABLET in 1 BOTTLE (68071-3885-6)
68071-3916-6	68071-3916	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20251118	N/A	ANDA	ANDA217566	NuCare Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	6 TABLET in 1 BOTTLE (68071-3916-6)
31722-079-01	31722-079	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20240507	N/A	ANDA	ANDA217566	Camber Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (31722-079-01)
31722-079-10	31722-079	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20240507	N/A	ANDA	ANDA217566	Camber Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	1000 TABLET in 1 BOTTLE (31722-079-10)