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
47335-616-90	47335-616	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	20 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-616-90)
47335-617-10	47335-617	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-617-10)
47335-617-30	47335-617	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-617-30)
47335-617-60	47335-617	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-617-60)
47335-617-90	47335-617	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	30 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-617-90)
47335-618-10	47335-618	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	40 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-10)
47335-618-30	47335-618	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	40 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-30)
47335-616-60	47335-616	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	20 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-616-60)
47335-618-90	47335-618	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	40 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-90)
47335-619-10	47335-619	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-619-10)
47335-619-30	47335-619	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-619-30)
47335-619-60	47335-619	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-619-60)
47335-619-90	47335-619	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	60 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-619-90)
47335-616-30	47335-616	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	20 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-616-30)
47335-616-10	47335-616	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	20 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-616-10)
47335-618-60	47335-618	HUMAN PRESCRIPTION DRUG	DRIZALMA SPRINKLE	Duloxetine	CAPSULE, DELAYED RELEASE	ORAL	20240610	N/A	NDA	NDA212516	SUN PHARMACEUTICAL INDUSTRIES, INC.	DULOXETINE HYDROCHLORIDE	40 mg/1	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-618-60)