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
21130-992-05	21130-992	HUMAN OTC DRUG	Ibuprofen	Ibuprofen Tablets USP, 200mg	TABLET	ORAL	20230808	N/A	ANDA	ANDA091237	BETTER LIVING BRANDS, LLC	IBUPROFEN	200 mg/1	1 BOTTLE in 1 CARTON (21130-992-05) / 50 TABLET in 1 BOTTLE
21130-992-53	21130-992	HUMAN OTC DRUG	Ibuprofen	Ibuprofen Tablets USP, 200mg	TABLET	ORAL	20230808	N/A	ANDA	ANDA091237	BETTER LIVING BRANDS, LLC	IBUPROFEN	200 mg/1	500 TABLET in 1 BOTTLE (21130-992-53)
11822-7893-5	11822-7893	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091237	RITE AID	IBUPROFEN	200 mg/1	100 TABLET, COATED in 1 BOTTLE (11822-7893-5)
11822-7893-2	11822-7893	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091237	RITE AID	IBUPROFEN	200 mg/1	50 TABLET, COATED in 1 BOTTLE (11822-7893-2)
11822-8925-5	11822-8925	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091237	RITE AID	IBUPROFEN	200 mg/1	100 TABLET, COATED in 1 BOTTLE (11822-8925-5)
11822-8925-9	11822-8925	HUMAN OTC DRUG	IBUPROFEN	IBUPROFEN	TABLET, COATED	ORAL	20200601	N/A	ANDA	ANDA091237	RITE AID	IBUPROFEN	200 mg/1	500 TABLET, COATED in 1 BOTTLE (11822-8925-9)