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）

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
71335-2488-5	71335-2488	HUMAN PRESCRIPTION DRUG	Phentermine Hydrochloride	Phentermine Hydrochloride	TABLET	ORAL	20240918	20280430	ANDA	ANDA200272	Bryant Ranch Prepack	PHENTERMINE HYDROCHLORIDE	37.5 mg/1	14 TABLET in 1 BOTTLE (71335-2488-5)
71335-2488-6	71335-2488	HUMAN PRESCRIPTION DRUG	Phentermine Hydrochloride	Phentermine Hydrochloride	TABLET	ORAL	20240918	20280430	ANDA	ANDA200272	Bryant Ranch Prepack	PHENTERMINE HYDROCHLORIDE	37.5 mg/1	60 TABLET in 1 BOTTLE (71335-2488-6)
71335-2488-7	71335-2488	HUMAN PRESCRIPTION DRUG	Phentermine Hydrochloride	Phentermine Hydrochloride	TABLET	ORAL	20240918	20280430	ANDA	ANDA200272	Bryant Ranch Prepack	PHENTERMINE HYDROCHLORIDE	37.5 mg/1	45 TABLET in 1 BOTTLE (71335-2488-7)
71335-2488-8	71335-2488	HUMAN PRESCRIPTION DRUG	Phentermine Hydrochloride	Phentermine Hydrochloride	TABLET	ORAL	20240918	20280430	ANDA	ANDA200272	Bryant Ranch Prepack	PHENTERMINE HYDROCHLORIDE	37.5 mg/1	2 TABLET in 1 BOTTLE (71335-2488-8)
71335-2488-9	71335-2488	HUMAN PRESCRIPTION DRUG	Phentermine Hydrochloride	Phentermine Hydrochloride	TABLET	ORAL	20240918	20280430	ANDA	ANDA200272	Bryant Ranch Prepack	PHENTERMINE HYDROCHLORIDE	37.5 mg/1	21 TABLET in 1 BOTTLE (71335-2488-9)