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=ANDA205087"
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
51407-272-10 51407-272 HUMAN PRESCRIPTION DRUG CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET ORAL 20190822 N/A ANDA ANDA205087 Golden State Medical Supply, Inc. CYPROHEPTADINE HYDROCHLORIDE 4 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (51407-272-10)
50742-190-01 50742-190 HUMAN PRESCRIPTION DRUG CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET ORAL 20150923 N/A ANDA ANDA205087 Ingenus Pharmaceuticals LLC CYPROHEPTADINE HYDROCHLORIDE 4 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01)
50742-190-10 50742-190 HUMAN PRESCRIPTION DRUG CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE HYDROCHLORIDE TABLET ORAL 20150923 N/A ANDA ANDA205087 Ingenus Pharmaceuticals LLC CYPROHEPTADINE HYDROCHLORIDE 4 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10)
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