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=NDA020067"
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
63629-2484-1 63629-2484 HUMAN PRESCRIPTION DRUG EC-NAPROXEN naproxen TABLET, DELAYED RELEASE ORAL 20220907 N/A NDA NDA020067 Bryant Ranch Prepack NAPROXEN 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63629-2484-1)
69437-415-01 69437-415 HUMAN PRESCRIPTION DRUG EC-Naprosyn naproxen TABLET, DELAYED RELEASE ORAL 20160601 N/A NDA NDA020067 Canton Laboratories NAPROXEN 375 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69437-415-01)
69437-416-01 69437-416 HUMAN PRESCRIPTION DRUG EC-Naprosyn naproxen TABLET, DELAYED RELEASE ORAL 20160601 N/A NDA NDA020067 Canton Laboratories NAPROXEN 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69437-416-01)
72162-1935-1 72162-1935 HUMAN PRESCRIPTION DRUG EC-NAPROXEN naproxen TABLET, DELAYED RELEASE ORAL 20240530 N/A NDA NDA020067 Bryant Ranch Prepack NAPROXEN 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1935-1)
69784-500-01 69784-500 HUMAN PRESCRIPTION DRUG EC-NAPROXEN naproxen TABLET, DELAYED RELEASE ORAL 20181015 N/A NDA NDA020067 Woodward Pharma Services LLC NAPROXEN 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69784-500-01)
69784-501-01 69784-501 HUMAN PRESCRIPTION DRUG EC-NAPROXEN naproxen TABLET, DELAYED RELEASE ORAL 20181015 N/A NDA NDA020067 Woodward Pharma Services LLC NAPROXEN 375 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69784-501-01)
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