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=ANDA207035"
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
59726-671-50 59726-671 HUMAN OTC DRUG Muscle Pain Relief Acetaminophen TABLET ORAL 20220204 20260204 ANDA ANDA207035 P & L Development, LLC ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 BOX (59726-671-50) / 24 TABLET in 1 BOTTLE, PLASTIC
11822-6690-5 11822-6690 HUMAN OTC DRUG Acetaminophen Extended Release Acetaminophen TABLET ORAL 20190812 20251231 ANDA ANDA207035 Rite Aid Corporation ACETAMINOPHEN 650 mg/1 225 TABLET in 1 BOTTLE, PLASTIC (11822-6690-5)
59726-669-10 59726-669 HUMAN OTC DRUG ArthritisPain Relief Acetaminophen TABLET ORAL 20210430 20260430 ANDA ANDA207035 P & L Development, LLC ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 BOX (59726-669-10) / 100 TABLET in 1 BOTTLE, PLASTIC
11822-6690-1 11822-6690 HUMAN OTC DRUG Acetaminophen Extended Release Acetaminophen TABLET ORAL 20190812 20251231 ANDA ANDA207035 Rite Aid Corporation ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 BOX (11822-6690-1) / 100 TABLET in 1 BOTTLE, PLASTIC
11822-6690-0 11822-6690 HUMAN OTC DRUG Acetaminophen Extended Release Acetaminophen TABLET ORAL 20190812 20251231 ANDA ANDA207035 Rite Aid Corporation ACETAMINOPHEN 650 mg/1 1 BOTTLE, PLASTIC in 1 BOX (11822-6690-0) / 50 TABLET in 1 BOTTLE, PLASTIC
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