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)
检索条件:" 注册申请号=ANDA202312"
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
42507-112-03 42507-112 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20260113 N/A ANDA ANDA202312 HYVEE INC IBUPROFEN 200 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (42507-112-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
42507-112-08 42507-112 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20260113 N/A ANDA ANDA202312 HYVEE INC IBUPROFEN 200 mg/1 225 TABLET, COATED in 1 BOTTLE, PLASTIC (42507-112-08)
21130-359-05 21130-359 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20200801 N/A ANDA ANDA202312 BETTER LIVING BRANDS LLC. IBUPROFEN 200 mg/1 50 TABLET, COATED in 1 BOTTLE (21130-359-05)
21130-359-10 21130-359 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20200801 N/A ANDA ANDA202312 BETTER LIVING BRANDS LLC. IBUPROFEN 200 mg/1 100 TABLET, COATED in 1 BOTTLE (21130-359-10)
62207-321-41 62207-321 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 24 TABLET in 1 BOTTLE (62207-321-41)
62207-321-42 62207-321 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 50 TABLET in 1 BOTTLE (62207-321-42)
62207-321-43 62207-321 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 100 TABLET in 1 BOTTLE (62207-321-43)
62207-321-46 62207-321 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 250 TABLET in 1 BOTTLE (62207-321-46)
62207-321-47 62207-321 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 500 TABLET in 1 BOTTLE (62207-321-47)
62207-321-48 62207-321 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 750 TABLET in 1 BOTTLE (62207-321-48)
63941-111-02 63941-111 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20200401 20280430 ANDA ANDA202312 VALU MERCHANDISERS COMPANY IBUPROFEN 200 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-111-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
21130-358-05 21130-358 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20190712 N/A ANDA ANDA202312 BETTER LIVING BRANDS LLC. IBUPROFEN 200 mg/1 50 TABLET, COATED in 1 BOTTLE (21130-358-05)
21130-358-10 21130-358 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20230630 N/A ANDA ANDA202312 BETTER LIVING BRANDS LLC. IBUPROFEN 200 mg/1 100 TABLET, COATED in 1 BOTTLE (21130-358-10)
21130-358-50 21130-358 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20190712 N/A ANDA ANDA202312 BETTER LIVING BRANDS LLC. IBUPROFEN 200 mg/1 500 TABLET, COATED in 1 BOTTLE (21130-358-50)
62207-320-41 62207-320 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 24 TABLET in 1 BOTTLE (62207-320-41)
62207-320-42 62207-320 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 50 TABLET in 1 BOTTLE (62207-320-42)
62207-320-43 62207-320 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 100 TABLET in 1 BOTTLE (62207-320-43)
62207-320-46 62207-320 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 250 TABLET in 1 BOTTLE (62207-320-46)
62207-320-47 62207-320 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 500 TABLET in 1 BOTTLE (62207-320-47)
62207-320-48 62207-320 HUMAN OTC DRUG IBUPROFEN IBUPROFEN TABLET ORAL 20191114 N/A ANDA ANDA202312 Granules India Limited IBUPROFEN 200 mg/1 750 TABLET in 1 BOTTLE (62207-320-48)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase