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=ANDA215932"
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
43598-008-01 43598-008 HUMAN OTC DRUG Guaifenesin 600 mg Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220901 N/A ANDA ANDA215932 Dr. Reddy¿s Laboratories Inc. GUAIFENESIN 600 mg/1 5 BLISTER PACK in 1 CARTON (43598-008-01) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-008-20)
43598-008-40 43598-008 HUMAN OTC DRUG Guaifenesin 600 mg Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220315 N/A ANDA ANDA215932 Dr. Reddy¿s Laboratories Inc. GUAIFENESIN 600 mg/1 2 BLISTER PACK in 1 CARTON (43598-008-40) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-008-20)
43598-009-25 43598-009 HUMAN OTC DRUG Guaifenesin 1200 mg Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220315 N/A ANDA ANDA215932 Dr. Reddy¿s Laboratories Inc. GUAIFENESIN 1200 mg/1 2 BLISTER PACK in 1 CARTON (43598-009-25) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-009-74)
43598-009-37 43598-009 HUMAN OTC DRUG Guaifenesin 1200 mg Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220901 N/A ANDA ANDA215932 Dr. Reddy¿s Laboratories Inc. GUAIFENESIN 1200 mg/1 3 BLISTER PACK in 1 CARTON (43598-009-37) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-009-74)
43598-108-37 43598-108 HUMAN OTC DRUG Guaifenesin 1200 mg Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220901 N/A ANDA ANDA215932 Dr. Reddy's Laboratories Inc. GUAIFENESIN 1200 mg/1 3 BLISTER PACK in 1 CARTON (43598-108-37) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
43598-110-01 43598-110 HUMAN OTC DRUG Guaifenesin 600 mg Guaifenesin TABLET, EXTENDED RELEASE ORAL 20220901 N/A ANDA ANDA215932 Dr. Reddy's Laboratories Inc. GUAIFENESIN 600 mg/1 5 BLISTER PACK in 1 CARTON (43598-110-01) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
51316-008-01 51316-008 HUMAN OTC DRUG Guaifenesin 600 mg Guaifenesin TABLET, EXTENDED RELEASE ORAL 20230501 N/A ANDA ANDA215932 CVS Pharmacy GUAIFENESIN 600 mg/1 5 BLISTER PACK in 1 CARTON (51316-008-01) / 20 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