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=ANDA076004"
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
60760-552-60 60760-552 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20151112 N/A ANDA ANDA076004 St. Mary’s Medical Park Pharmacy ETODOLAC 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-552-60)
43063-578-20 43063-578 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20091028 N/A ANDA ANDA076004 PD-Rx Pharmaceuticals, Inc. ETODOLAC 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-578-20)
43063-671-30 43063-671 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20180116 N/A ANDA ANDA076004 PD-Rx Pharmaceuticals, Inc. ETODOLAC 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-671-30)
43063-856-20 43063-856 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA076004 PD-Rx Pharmaceuticals, Inc. ETODOLAC 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-856-20)
43063-856-30 43063-856 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20180627 N/A ANDA ANDA076004 PD-Rx Pharmaceuticals, Inc. ETODOLAC 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-856-30)
43063-856-60 43063-856 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA076004 PD-Rx Pharmaceuticals, Inc. ETODOLAC 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-856-60)
71335-0126-8 71335-0126 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20240905 N/A ANDA ANDA076004 Bryant Ranch Prepack ETODOLAC 400 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0126-8)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase