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=ANDA211544"
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
79481-0184-8 79481-0184 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET ORAL 20230717 N/A ANDA ANDA211544 MEIJER, INC. ACETAMINOPHEN 650 mg/1 24 TABLET in 1 BOTTLE (79481-0184-8)
81522-200-03 81522-200 HUMAN OTC DRUG 8HR Arthritis Pain Acetaminophen TABLET, EXTENDED RELEASE ORAL 20231116 N/A ANDA ANDA211544 FSA STORE INC. ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (81522-200-03) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
11822-5019-2 11822-5019 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET, FILM COATED, EXTENDED RELEASE ORAL 20241101 N/A ANDA ANDA211544 RITE AID ACETAMINOPHEN 650 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (11822-5019-2)
11822-5019-3 11822-5019 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET, FILM COATED, EXTENDED RELEASE ORAL 20241101 N/A ANDA ANDA211544 RITE AID ACETAMINOPHEN 650 mg/1 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (11822-5019-3)
83324-082-50 83324-082 HUMAN OTC DRUG 8 Hour Pain Relief Acetaminophen TABLET, EXTENDED RELEASE ORAL 20240501 N/A ANDA ANDA211544 CHAIN DRUG MARKETING ASSOCIATION, INC. ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (83324-082-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
0363-9992-24 0363-9992 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190928 N/A ANDA ANDA211544 WALGREENS ACETAMINOPHEN 650 mg/1 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-9992-24)
69848-015-10 69848-015 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191231 N/A ANDA ANDA211544 Granules USA, Inc. ACETAMINOPHEN 650 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69848-015-10)
69848-015-24 69848-015 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221130 N/A ANDA ANDA211544 Granules USA, Inc. ACETAMINOPHEN 650 mg/1 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69848-015-24)
53329-197-29 53329-197 HUMAN OTC DRUG Medline acetaminophen TABLET, EXTENDED RELEASE ORAL 20240701 N/A ANDA ANDA211544 Medline Industries, LP ACETAMINOPHEN 650 mg/1 50 TABLET, EXTENDED RELEASE in 1 BOTTLE (53329-197-29)
85828-200-01 85828-200 HUMAN OTC DRUG Arthritis Pain Acetaminophen TABLET, EXTENDED RELEASE ORAL 20260218 N/A ANDA ANDA211544 Grocery Outlet, Inc. ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (85828-200-01) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
79481-0183-1 79481-0183 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET ORAL 20230717 N/A ANDA ANDA211544 MEIJER DISTRIBUTION INC ACETAMINOPHEN 650 mg/1 100 TABLET in 1 BOTTLE (79481-0183-1)
79481-0183-2 79481-0183 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET ORAL 20230717 N/A ANDA ANDA211544 MEIJER DISTRIBUTION INC ACETAMINOPHEN 650 mg/1 225 TABLET in 1 BOTTLE (79481-0183-2)
79481-0183-4 79481-0183 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET ORAL 20230717 N/A ANDA ANDA211544 MEIJER DISTRIBUTION INC ACETAMINOPHEN 650 mg/1 400 TABLET in 1 BOTTLE (79481-0183-4)
79481-0183-5 79481-0183 HUMAN OTC DRUG Acetaminophen Acetaminophen TABLET ORAL 20230717 N/A ANDA ANDA211544 MEIJER DISTRIBUTION INC ACETAMINOPHEN 650 mg/1 150 TABLET in 1 BOTTLE (79481-0183-5)
46122-630-71 46122-630 HUMAN OTC DRUG 8 Hour Pain Relief Acetaminophen TABLET, EXTENDED RELEASE ORAL 20240827 N/A ANDA ANDA211544 AMERISOURCE BERGEN ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 PACKAGE (46122-630-71) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
46122-630-78 46122-630 HUMAN OTC DRUG 8 Hour Pain Relief Acetaminophen TABLET, EXTENDED RELEASE ORAL 20200113 N/A ANDA ANDA211544 AMERISOURCE BERGEN ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (46122-630-78) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
70010-160-01 70010-160 HUMAN OTC DRUG ACETAMINOPHEN ACETAMINOPHEN TABLET, EXTENDED RELEASE ORAL 20220215 N/A ANDA ANDA211544 Granules Pharmaceuticals Inc. ACETAMINOPHEN 650 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-160-01)
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