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
67184-0523-1	67184-0523	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211117	N/A	ANDA	ANDA210420	Qilu Pharmaceutical Co., Ltd.	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67184-0523-1)
67184-0523-2	67184-0523	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211117	N/A	ANDA	ANDA210420	Qilu Pharmaceutical Co., Ltd.	TADALAFIL	2.5 mg/1	2 BLISTER PACK in 1 CARTON (67184-0523-2) / 15 TABLET, FILM COATED in 1 BLISTER PACK
67184-0524-1	67184-0524	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211117	N/A	ANDA	ANDA210420	Qilu Pharmaceutical Co., Ltd.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67184-0524-1)
67184-0524-2	67184-0524	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211117	N/A	ANDA	ANDA210420	Qilu Pharmaceutical Co., Ltd.	TADALAFIL	5 mg/1	2 BLISTER PACK in 1 CARTON (67184-0524-2) / 15 TABLET, FILM COATED in 1 BLISTER PACK
67184-0525-2	67184-0525	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211117	N/A	ANDA	ANDA210420	Qilu Pharmaceutical Co., Ltd.	TADALAFIL	10 mg/1	1 BLISTER PACK in 1 CARTON (67184-0525-2) / 7 TABLET, FILM COATED in 1 BLISTER PACK
67184-0526-1	67184-0526	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211117	N/A	ANDA	ANDA210420	Qilu Pharmaceutical Co., Ltd.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67184-0526-1)
67184-0526-2	67184-0526	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211117	N/A	ANDA	ANDA210420	Qilu Pharmaceutical Co., Ltd.	TADALAFIL	20 mg/1	1 BLISTER PACK in 1 CARTON (67184-0526-2) / 7 TABLET, FILM COATED in 1 BLISTER PACK
80425-0443-1	80425-0443	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20241015	N/A	ANDA	ANDA210420	Advanced Rx of Tennessee, LLC	TADALAFIL	20 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (80425-0443-1)
71205-400-10	71205-400	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200207	N/A	ANDA	ANDA210420	Proficient Rx LP	TADALAFIL	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-400-10)
24979-727-02	24979-727	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240407	N/A	ANDA	ANDA210420	Upsher-Smith Laboratories, LLC	TADALAFIL	2.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (24979-727-02)
24979-727-06	24979-727	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240407	N/A	ANDA	ANDA210420	Upsher-Smith Laboratories, LLC	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (24979-727-06)
24979-728-02	24979-728	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240407	N/A	ANDA	ANDA210420	Upsher-Smith Laboratories, LLC	TADALAFIL	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (24979-728-02)
24979-728-06	24979-728	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240407	N/A	ANDA	ANDA210420	Upsher-Smith Laboratories, LLC	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (24979-728-06)
24979-729-06	24979-729	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240407	N/A	ANDA	ANDA210420	Upsher-Smith Laboratories, LLC	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (24979-729-06)
24979-729-69	24979-729	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240407	N/A	ANDA	ANDA210420	Upsher-Smith Laboratories, LLC	TADALAFIL	10 mg/1	250 TABLET, FILM COATED in 1 BOTTLE (24979-729-69)
24979-730-06	24979-730	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240407	N/A	ANDA	ANDA210420	Upsher-Smith Laboratories, LLC	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (24979-730-06)
24979-730-44	24979-730	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240407	N/A	ANDA	ANDA210420	Upsher-Smith Laboratories, LLC	TADALAFIL	20 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (24979-730-44)