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
68788-8438-3	68788-8438	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230428	N/A	ANDA	ANDA213794	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	30 TABLET in 1 BOTTLE (68788-8438-3)
68788-8438-5	68788-8438	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230428	N/A	ANDA	ANDA213794	Preferred Pharmaceuticals Inc.	IBUPROFEN	400 mg/1	50 TABLET in 1 BOTTLE (68788-8438-5)
70518-4341-0	70518-4341	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250516	N/A	ANDA	ANDA213794	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	30 TABLET in 1 BLISTER PACK (70518-4341-0)
70518-4341-1	70518-4341	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250819	N/A	ANDA	ANDA213794	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	30 TABLET in 1 BLISTER PACK (70518-4341-1)
71610-897-70	71610-897	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250402	N/A	ANDA	ANDA213794	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	120 TABLET in 1 BOTTLE (71610-897-70)
71610-897-92	71610-897	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250402	N/A	ANDA	ANDA213794	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	270 TABLET in 1 BOTTLE (71610-897-92)
71610-897-80	71610-897	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250402	N/A	ANDA	ANDA213794	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	180 TABLET in 1 BOTTLE (71610-897-80)
71610-897-53	71610-897	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250402	N/A	ANDA	ANDA213794	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (71610-897-53)
71610-897-60	71610-897	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20250402	N/A	ANDA	ANDA213794	Aphena Pharma Solutions - Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (71610-897-60)
76420-575-01	76420-575	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230720	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (76420-575-01)
76420-576-01	76420-576	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230720	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	100 TABLET in 1 BOTTLE (76420-576-01)
76420-576-02	76420-576	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20231006	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	2 TABLET in 1 BOTTLE (76420-576-02)
76420-576-05	76420-576	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20231006	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	500 TABLET in 1 BOTTLE (76420-576-05)
76420-576-10	76420-576	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20231006	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	10 TABLET in 1 BOTTLE (76420-576-10)
76420-576-20	76420-576	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20231006	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	20 TABLET in 1 BOTTLE (76420-576-20)
76420-576-30	76420-576	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230720	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	30 TABLET in 1 BOTTLE (76420-576-30)
76420-576-60	76420-576	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230720	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	60 TABLET in 1 BOTTLE (76420-576-60)
76420-576-90	76420-576	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230720	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	600 mg/1	90 TABLET in 1 BOTTLE (76420-576-90)
76420-577-01	76420-577	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230720	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (76420-577-01)
76420-577-30	76420-577	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230720	N/A	ANDA	ANDA213794	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (76420-577-30)