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=ANDA074140"
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
70010-139-01 70010-139 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 500 mg/1 100 TABLET in 1 BOTTLE (70010-139-01)
70010-139-05 70010-139 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 500 mg/1 500 TABLET in 1 BOTTLE (70010-139-05)
70010-139-10 70010-139 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210415 N/A ANDA ANDA074140 Granules Pharmaceuticals Inc. NAPROXEN 500 mg/1 1000 TABLET in 1 BOTTLE (70010-139-10)
70518-4514-0 70518-4514 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20251103 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN 250 mg/1 30 TABLET in 1 BLISTER PACK (70518-4514-0)
70518-4439-0 70518-4439 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250813 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN 500 mg/1 12 TABLET in 1 BOTTLE, PLASTIC (70518-4439-0)
70518-4439-1 70518-4439 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250924 N/A ANDA ANDA074140 REMEDYREPACK INC. NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (70518-4439-1)
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