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
63304-131-01	63304-131	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63304-131-01)
63304-131-10	63304-131	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	75 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (63304-131-10)
63304-173-03	63304-173	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	150 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63304-173-03)
63304-173-10	63304-173	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	150 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (63304-173-10)
63304-173-30	63304-173	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-173-30)
63304-173-69	63304-173	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	150 mg/1	1 BLISTER PACK in 1 CARTON (63304-173-69) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-173-11)
63304-132-04	63304-132	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	100 mg/1	250 TABLET, FILM COATED in 1 BOTTLE (63304-132-04)
63304-132-10	63304-132	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (63304-132-10)
63304-132-50	63304-132	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (63304-132-50)
63304-130-10	63304-130	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180806	N/A	ANDA	ANDA065356	Sun Pharmaceutical Industries Inc.	DOXYCYCLINE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (63304-130-10)