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
71610-714-30	71610-714	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20230612	N/A	ANDA	ANDA213335	Aphena Pharma Solutions - Tennessee, LLC	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	30 TABLET in 1 BOTTLE (71610-714-30)
71610-714-53	71610-714	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20230612	N/A	ANDA	ANDA213335	Aphena Pharma Solutions - Tennessee, LLC	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	60 TABLET in 1 BOTTLE (71610-714-53)
71610-714-60	71610-714	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20230612	N/A	ANDA	ANDA213335	Aphena Pharma Solutions - Tennessee, LLC	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	90 TABLET in 1 BOTTLE (71610-714-60)
71610-714-70	71610-714	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20230612	N/A	ANDA	ANDA213335	Aphena Pharma Solutions - Tennessee, LLC	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	120 TABLET in 1 BOTTLE (71610-714-70)
71610-714-80	71610-714	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20230612	N/A	ANDA	ANDA213335	Aphena Pharma Solutions - Tennessee, LLC	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	180 TABLET in 1 BOTTLE (71610-714-80)
71610-714-90	71610-714	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20230612	N/A	ANDA	ANDA213335	Aphena Pharma Solutions - Tennessee, LLC	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	240 TABLET in 1 BOTTLE (71610-714-90)
0406-1236-01	0406-1236	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20201030	N/A	ANDA	ANDA213335	SpecGx LLC	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	100 TABLET in 1 BOTTLE (0406-1236-01)
0406-1236-10	0406-1236	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20201030	N/A	ANDA	ANDA213335	SpecGx LLC	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	1000 TABLET in 1 BOTTLE (0406-1236-10)
60687-890-01	60687-890	HUMAN PRESCRIPTION DRUG	Diphenoxylate Hydrochloride and Atropine Sulfate	diphenoxylate hydrochloride and atropine sulfate	TABLET	ORAL	20250801	N/A	ANDA	ANDA213335	American Health Packaging	ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE	.025 mg/1; 2.5 mg/1	100 BLISTER PACK in 1 CARTON (60687-890-01) / 1 TABLET in 1 BLISTER PACK (60687-890-11)