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
72789-309-01	72789-309	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20230315	N/A	ANDA	ANDA065134	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-01)
72789-309-60	72789-309	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20230327	N/A	ANDA	ANDA065134	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-60)
72789-309-93	72789-309	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20230327	N/A	ANDA	ANDA065134	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-93)
53489-647-10	53489-647	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20050513	N/A	ANDA	ANDA065134	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-10)
53489-647-90	53489-647	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20050513	N/A	ANDA	ANDA065134	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-90)
53489-647-01	53489-647	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20050513	N/A	ANDA	ANDA065134	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-01)
53489-647-03	53489-647	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20050513	N/A	ANDA	ANDA065134	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-03)
53489-647-05	53489-647	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20050513	N/A	ANDA	ANDA065134	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-05)
53489-647-06	53489-647	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20050513	N/A	ANDA	ANDA065134	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-06)
53489-647-07	53489-647	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20050513	N/A	ANDA	ANDA065134	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-07)