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
72789-276-10	72789-276	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20230713	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-276-10)
72789-319-06	72789-319	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20231218	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-06)
72789-319-28	72789-319	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20230426	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-28)
72789-319-30	72789-319	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20230808	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-30)
72789-319-60	72789-319	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20230606	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-60)
72789-319-07	72789-319	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20231206	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-07)
72789-319-10	72789-319	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20230329	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-10)
72789-319-14	72789-319	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20250404	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-14)
72789-419-14	72789-419	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20240703	N/A	ANDA	ANDA062677	PD-Rx Pharmaceuticals, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-419-14)
53489-120-60	53489-120	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	19860710	N/A	ANDA	ANDA062677	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-60)
53489-120-01	53489-120	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20231205	N/A	ANDA	ANDA062677	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-01)
53489-120-02	53489-120	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	19860710	N/A	ANDA	ANDA062677	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-02)
53489-120-05	53489-120	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	19860710	N/A	ANDA	ANDA062677	Sun Pharmaceutical Industries, Inc.	DOXYCYCLINE HYCLATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-05)