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
72789-212-30	72789-212	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211019	N/A	ANDA	ANDA078329	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-30)
72789-212-40	72789-212	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220103	N/A	ANDA	ANDA078329	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-40)
72789-212-90	72789-212	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211025	N/A	ANDA	ANDA078329	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-90)
72789-218-30	72789-218	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20251009	N/A	ANDA	ANDA078329	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-218-30)
72789-212-10	72789-212	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220802	N/A	ANDA	ANDA078329	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-10)
72789-212-15	72789-212	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211027	N/A	ANDA	ANDA078329	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-15)
72789-212-20	72789-212	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211119	N/A	ANDA	ANDA078329	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-20)
76420-415-60	76420-415	HUMAN PRESCRIPTION DRUG	Ibuprofen	ibuprofen	TABLET	ORAL	20250802	N/A	ANDA	ANDA078329	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (76420-415-60)
76420-415-30	76420-415	HUMAN PRESCRIPTION DRUG	Ibuprofen	ibuprofen	TABLET	ORAL	20250802	N/A	ANDA	ANDA078329	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (76420-415-30)
76420-415-90	76420-415	HUMAN PRESCRIPTION DRUG	Ibuprofen	ibuprofen	TABLET	ORAL	20250802	N/A	ANDA	ANDA078329	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (76420-415-90)
76420-415-01	76420-415	HUMAN PRESCRIPTION DRUG	Ibuprofen	ibuprofen	TABLET	ORAL	20250802	N/A	ANDA	ANDA078329	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (76420-415-01)
76420-415-05	76420-415	HUMAN PRESCRIPTION DRUG	Ibuprofen	ibuprofen	TABLET	ORAL	20250802	N/A	ANDA	ANDA078329	Asclemed USA, Inc.	IBUPROFEN	800 mg/1	500 TABLET in 1 BOTTLE (76420-415-05)