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
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)
63187-736-20 63187-736 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20160801 N/A ANDA ANDA076004 Proficient Rx LP ETODOLAC 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (63187-736-20)
63187-736-30 63187-736 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20160801 N/A ANDA ANDA076004 Proficient Rx LP ETODOLAC 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-736-30)
63187-736-60 63187-736 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20160801 N/A ANDA ANDA076004 Proficient Rx LP ETODOLAC 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-736-60)
63187-736-90 63187-736 HUMAN PRESCRIPTION DRUG Etodolac Etodolac TABLET, FILM COATED ORAL 20160801 N/A ANDA ANDA076004 Proficient Rx LP ETODOLAC 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-736-90)
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