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=ANDA200900"
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
71335-2242-5 71335-2242 HUMAN PRESCRIPTION DRUG PROGESTERONE PROGESTERONE CAPSULE ORAL 20230922 N/A ANDA ANDA200900 Bryant Ranch Prepack PROGESTERONE 200 mg/1 100 CAPSULE in 1 BOTTLE (71335-2242-5)
71335-2242-6 71335-2242 HUMAN PRESCRIPTION DRUG PROGESTERONE PROGESTERONE CAPSULE ORAL 20230922 N/A ANDA ANDA200900 Bryant Ranch Prepack PROGESTERONE 200 mg/1 6 CAPSULE in 1 BOTTLE (71335-2242-6)
71335-2242-7 71335-2242 HUMAN PRESCRIPTION DRUG PROGESTERONE PROGESTERONE CAPSULE ORAL 20230922 N/A ANDA ANDA200900 Bryant Ranch Prepack PROGESTERONE 200 mg/1 60 CAPSULE in 1 BOTTLE (71335-2242-7)
71335-2242-8 71335-2242 HUMAN PRESCRIPTION DRUG PROGESTERONE PROGESTERONE CAPSULE ORAL 20230922 N/A ANDA ANDA200900 Bryant Ranch Prepack PROGESTERONE 200 mg/1 180 CAPSULE in 1 BOTTLE (71335-2242-8)
71335-2242-9 71335-2242 HUMAN PRESCRIPTION DRUG PROGESTERONE PROGESTERONE CAPSULE ORAL 20230922 N/A ANDA ANDA200900 Bryant Ranch Prepack PROGESTERONE 200 mg/1 10 CAPSULE in 1 BOTTLE (71335-2242-9)
69452-234-20 69452-234 HUMAN PRESCRIPTION DRUG PROGESTERONE PROGESTERONE CAPSULE ORAL 20181128 N/A ANDA ANDA200900 Bionpharma Inc. PROGESTERONE 200 mg/1 100 CAPSULE in 1 BOTTLE (69452-234-20)
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