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
71337-046-01	71337-046	HUMAN PRESCRIPTION DRUG	DICLOFENAC POTASSIUM	diclofenac potassium, film coated	TABLET	ORAL	20230626	N/A	ANDA	ANDA215787	Havix Group Inc d-b-a Aavis Pharmaceuticals	DICLOFENAC POTASSIUM	50 mg/1	100 TABLET in 1 BOTTLE (71337-046-01)
71337-046-05	71337-046	HUMAN PRESCRIPTION DRUG	DICLOFENAC POTASSIUM	diclofenac potassium, film coated	TABLET	ORAL	20230626	N/A	ANDA	ANDA215787	Havix Group Inc d-b-a Aavis Pharmaceuticals	DICLOFENAC POTASSIUM	50 mg/1	500 TABLET in 1 BOTTLE (71337-046-05)
80425-0457-1	80425-0457	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20241021	N/A	ANDA	ANDA215787	Advanced Rx of Tennessee, LLC	DICLOFENAC POTASSIUM	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0457-1)
80425-0457-2	80425-0457	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20241021	N/A	ANDA	ANDA215787	Advanced Rx of Tennessee, LLC	DICLOFENAC POTASSIUM	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0457-2)
80425-0457-3	80425-0457	HUMAN PRESCRIPTION DRUG	Diclofenac Potassium	diclofenac potassium	TABLET, FILM COATED	ORAL	20241021	N/A	ANDA	ANDA215787	Advanced Rx of Tennessee, LLC	DICLOFENAC POTASSIUM	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0457-3)
74157-016-60	74157-016	HUMAN PRESCRIPTION DRUG	DICLOFENAC POTASSIUM	diclofenac potassium, film coated	TABLET	ORAL	20241001	N/A	ANDA	ANDA215787	INA Pharmaceutics Inc,	DICLOFENAC POTASSIUM	25 mg/1	60 TABLET in 1 BOTTLE (74157-016-60)