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=ANDA209254"
符合检索条件的记录共 13 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
51316-071-68 51316-071 HUMAN OTC DRUG GUAIFENESIN guaifenesin TABLET, EXTENDED RELEASE ORAL 20221007 N/A ANDA ANDA209254 CVS GUAIFENESIN 600 mg/1 1 BLISTER PACK in 1 CARTON (51316-071-68) / 68 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
41415-996-20 41415-996 HUMAN OTC DRUG GUAIFENESIN Guaifenesin TABLET, EXTENDED RELEASE ORAL 20180208 N/A ANDA ANDA209254 Publix Super Markets, Inc GUAIFENESIN 600 mg/1 1 BLISTER PACK in 1 CARTON (41415-996-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
51660-567-54 51660-567 HUMAN OTC DRUG Guaifenesin Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220401 N/A ANDA ANDA209254 Ohm Laboratories, Inc. GUAIFENESIN 1200 mg/1 14 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-54)
51660-567-58 51660-567 HUMAN OTC DRUG Guaifenesin Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220401 N/A ANDA ANDA209254 Ohm Laboratories, Inc. GUAIFENESIN 1200 mg/1 56 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-58)
51660-567-86 51660-567 HUMAN OTC DRUG Guaifenesin Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220401 N/A ANDA ANDA209254 Ohm Laboratories, Inc. GUAIFENESIN 1200 mg/1 28 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-86)
79903-124-20 79903-124 HUMAN OTC DRUG GUAIFENESIN Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220428 N/A ANDA ANDA209254 Walmart Stores, Inc. GUAIFENESIN 600 mg/1 1 BLISTER PACK in 1 CARTON (79903-124-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
51660-566-21 51660-566 HUMAN OTC DRUG Guaifenesin Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220401 N/A ANDA ANDA209254 Ohm Laboratories, Inc. GUAIFENESIN 600 mg/1 20 TABLET, EXTENDED RELEASE in 1 CARTON (51660-566-21)
51660-566-41 51660-566 HUMAN OTC DRUG Guaifenesin Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220401 N/A ANDA ANDA209254 Ohm Laboratories, Inc. GUAIFENESIN 600 mg/1 40 TABLET, EXTENDED RELEASE in 1 CARTON (51660-566-41)
30142-962-14 30142-962 HUMAN OTC DRUG Guaifenesin Extended Release Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220420 N/A ANDA ANDA209254 Kroger Company GUAIFENESIN 1200 mg/1 1 BLISTER PACK in 1 CARTON (30142-962-14) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
68196-996-56 68196-996 HUMAN OTC DRUG Guaifenesin Extended Release Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220112 N/A ANDA ANDA209254 SAM'S WEST INC GUAIFENESIN 1200 mg/1 4 BLISTER PACK in 1 CARTON (68196-996-56) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
46122-750-51 46122-750 HUMAN OTC DRUG Guaifenesin Guaifenesin TABLET, EXTENDED RELEASE ORAL 20230811 N/A ANDA ANDA209254 AMERISOURCE BERGEN GUAIFENESIN 600 mg/1 2 BLISTER PACK in 1 CARTON (46122-750-51) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
30142-961-20 30142-961 HUMAN OTC DRUG GUAIFENESIN Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220428 N/A ANDA ANDA209254 Kroger Company GUAIFENESIN 600 mg/1 1 BLISTER PACK in 1 CARTON (30142-961-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
41415-997-14 41415-997 HUMAN OTC DRUG Guaifenesin Extended Release Guaifenesin TABLET, EXTENDED RELEASE ORAL 20171210 N/A ANDA ANDA209254 PUBLIX SUPER MARKETS, INC GUAIFENESIN 1200 mg/1 1 BLISTER PACK in 1 CARTON (41415-997-14) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase