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=ANDA203436"
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
10702-067-10 10702-067 HUMAN PRESCRIPTION DRUG Phentermine Hydrochloride Phentermine Hydrochloride TABLET ORAL 20180329 N/A ANDA ANDA203436 KVK-TECH, Inc. PHENTERMINE HYDROCHLORIDE 8 mg/1 1000 TABLET in 1 BOTTLE (10702-067-10)
10702-067-05 10702-067 HUMAN PRESCRIPTION DRUG Phentermine Hydrochloride Phentermine Hydrochloride TABLET ORAL 20180329 N/A ANDA ANDA203436 KVK-TECH, Inc. PHENTERMINE HYDROCHLORIDE 8 mg/1 5000 TABLET in 1 BOTTLE (10702-067-05)
10702-067-03 10702-067 HUMAN PRESCRIPTION DRUG Phentermine Hydrochloride Phentermine Hydrochloride TABLET ORAL 20180329 N/A ANDA ANDA203436 KVK-TECH, Inc. PHENTERMINE HYDROCHLORIDE 8 mg/1 30 TABLET in 1 BOTTLE (10702-067-03)
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