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
63304-028-30	63304-028	HUMAN PRESCRIPTION DRUG	Dapagliflozin and Metformin Hydrochloride	Dapagliflozin and Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260406	N/A	ANDA	ANDA211491	Sun Pharmaceutical Industries, Inc.	DAPAGLIFLOZIN; METFORMIN HYDROCHLORIDE	10 mg/1; 1000 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-028-30)
63304-028-54	63304-028	HUMAN PRESCRIPTION DRUG	Dapagliflozin and Metformin Hydrochloride	Dapagliflozin and Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260406	N/A	ANDA	ANDA211491	Sun Pharmaceutical Industries, Inc.	DAPAGLIFLOZIN; METFORMIN HYDROCHLORIDE	10 mg/1; 1000 mg/1	400 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-028-54)
63304-027-30	63304-027	HUMAN PRESCRIPTION DRUG	Dapagliflozin and Metformin Hydrochloride	Dapagliflozin and Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260406	N/A	ANDA	ANDA211491	Sun Pharmaceutical Industries, Inc.	DAPAGLIFLOZIN; METFORMIN HYDROCHLORIDE	10 mg/1; 500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-027-30)
63304-027-54	63304-027	HUMAN PRESCRIPTION DRUG	Dapagliflozin and Metformin Hydrochloride	Dapagliflozin and Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260406	N/A	ANDA	ANDA211491	Sun Pharmaceutical Industries, Inc.	DAPAGLIFLOZIN; METFORMIN HYDROCHLORIDE	10 mg/1; 500 mg/1	400 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-027-54)
63304-026-30	63304-026	HUMAN PRESCRIPTION DRUG	Dapagliflozin and Metformin Hydrochloride	Dapagliflozin and Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260406	N/A	ANDA	ANDA211491	Sun Pharmaceutical Industries, Inc.	DAPAGLIFLOZIN; METFORMIN HYDROCHLORIDE	5 mg/1; 1000 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-026-30)
63304-026-54	63304-026	HUMAN PRESCRIPTION DRUG	Dapagliflozin and Metformin Hydrochloride	Dapagliflozin and Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260406	N/A	ANDA	ANDA211491	Sun Pharmaceutical Industries, Inc.	DAPAGLIFLOZIN; METFORMIN HYDROCHLORIDE	5 mg/1; 1000 mg/1	400 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-026-54)
63304-026-62	63304-026	HUMAN PRESCRIPTION DRUG	Dapagliflozin and Metformin Hydrochloride	Dapagliflozin and Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260406	N/A	ANDA	ANDA211491	Sun Pharmaceutical Industries, Inc.	DAPAGLIFLOZIN; METFORMIN HYDROCHLORIDE	5 mg/1; 1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-026-62)