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=NDA209501"
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
58151-247-93 58151-247 HUMAN PRESCRIPTION DRUG Lyrica CR PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240711 N/A NDA NDA209501 Viatris Specialty LLC PREGABALIN 330 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (58151-247-93)
0071-1029-01 0071-1029 HUMAN PRESCRIPTION DRUG Lyrica CR PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180101 20240930 NDA NDA209501 Parke-Davis Div of Pfizer Inc PREGABALIN 330 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0071-1029-01)
0071-1027-01 0071-1027 HUMAN PRESCRIPTION DRUG Lyrica CR PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180101 N/A NDA NDA209501 Parke-Davis Div of Pfizer Inc PREGABALIN 165 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0071-1027-01)
0071-1026-01 0071-1026 HUMAN PRESCRIPTION DRUG Lyrica CR PREGABALIN TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180101 N/A NDA NDA209501 Parke-Davis Div of Pfizer Inc PREGABALIN 82.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0071-1026-01)
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