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=ANDA213420"
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
76162-523-01 76162-523 HUMAN OTC DRUG Topcare Mucus ER Guaifenesin TABLET, MULTILAYER, EXTENDED RELEASE ORAL 20220909 N/A ANDA ANDA213420 Topco Associates LLC GUAIFENESIN 1200 mg/1 1 BLISTER PACK in 1 CARTON (76162-523-01) / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
69848-017-02 69848-017 HUMAN OTC DRUG Guaifenesin Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220106 N/A ANDA ANDA213420 GRANULES USA, INC. GUAIFENESIN 600 mg/1 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69848-017-02)
72559-013-11 72559-013 HUMAN OTC DRUG Curist Mucus Relief Maximum Strength Guaifenesin TABLET, EXTENDED RELEASE ORAL 20210723 N/A ANDA ANDA213420 Little Pharma, Inc. GUAIFENESIN 1200 mg/1 6 BLISTER PACK in 1 CARTON (72559-013-11) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
72559-013-28 72559-013 HUMAN OTC DRUG Curist Mucus Relief Maximum Strength Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220406 N/A ANDA ANDA213420 Little Pharma, Inc. GUAIFENESIN 1200 mg/1 150 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-28)
83324-097-20 83324-097 HUMAN OTC DRUG Mucus Relief Guaifenesin TABLET, EXTENDED RELEASE ORAL 20240718 N/A ANDA ANDA213420 CHAIN DRUG MARKETING ASSOCIATION, INC. GUAIFENESIN 600 mg/1 1 BLISTER PACK in 1 CARTON (83324-097-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
81179-007-04 81179-007 HUMAN OTC DRUG EXPECTORANT GUAIFENESIN EXTENDED-RELEASE GUAIFENESIN TABLET ORAL 20210412 N/A ANDA ANDA213420 YET HEALTH GROUP LLC GUAIFENESIN 1200 mg/1 5 BLISTER PACK in 1 PACKAGE (81179-007-04) / 14 TABLET in 1 BLISTER PACK
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