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=ANDA214475"
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
71205-828-30 71205-828 HUMAN PRESCRIPTION DRUG FENOPROFEN CALCIUM FENOPROFEN CALCIUM CAPSULE ORAL 20230815 N/A ANDA ANDA214475 Proficient Rx LP FENOPROFEN CALCIUM 400 mg/1 30 CAPSULE in 1 BOTTLE (71205-828-30)
71205-828-60 71205-828 HUMAN PRESCRIPTION DRUG FENOPROFEN CALCIUM FENOPROFEN CALCIUM CAPSULE ORAL 20230815 N/A ANDA ANDA214475 Proficient Rx LP FENOPROFEN CALCIUM 400 mg/1 60 CAPSULE in 1 BOTTLE (71205-828-60)
71205-828-90 71205-828 HUMAN PRESCRIPTION DRUG FENOPROFEN CALCIUM FENOPROFEN CALCIUM CAPSULE ORAL 20230815 N/A ANDA ANDA214475 Proficient Rx LP FENOPROFEN CALCIUM 400 mg/1 90 CAPSULE in 1 BOTTLE (71205-828-90)
16571-886-01 16571-886 HUMAN PRESCRIPTION DRUG FENOPROFEN CALCIUM FENOPROFEN CALCIUM CAPSULE ORAL 20240726 N/A ANDA ANDA214475 Rising Pharma Holdings, Inc. FENOPROFEN CALCIUM 200 mg/1 100 CAPSULE in 1 BOTTLE (16571-886-01)
16571-887-01 16571-887 HUMAN PRESCRIPTION DRUG FENOPROFEN CALCIUM FENOPROFEN CALCIUM CAPSULE ORAL 20240726 N/A ANDA ANDA214475 Rising Pharma Holdings, Inc. FENOPROFEN CALCIUM 300 mg/1 100 CAPSULE in 1 BOTTLE (16571-887-01)
16571-688-09 16571-688 HUMAN PRESCRIPTION DRUG FENOPROFEN CALCIUM FENOPROFEN CALCIUM CAPSULE ORAL 20220801 N/A ANDA ANDA214475 Rising Pharma Holdings, Inc. FENOPROFEN CALCIUM 400 mg/1 90 CAPSULE in 1 BOTTLE (16571-688-09)
71993-308-90 71993-308 HUMAN PRESCRIPTION DRUG FENOPROFEN CALCIUM FENOPROFEN CALCIUM CAPSULE ORAL 20240326 N/A ANDA ANDA214475 Atland Pharmaceuticals, LLC FENOPROFEN CALCIUM 400 mg/1 90 CAPSULE in 1 BOTTLE (71993-308-90)
61825-311-10 61825-311 HUMAN PRESCRIPTION DRUG FENOPRON TM FENOPROFEN CALCIUM CAPSULE ORAL 20241210 N/A ANDA ANDA214475 Galt Pharmaceuticals, LLC FENOPROFEN CALCIUM 300 mg/1 100 CAPSULE in 1 BOTTLE (61825-311-10)
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