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
87063-014-01	87063-014	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (87063-014-01)
87063-014-05	87063-014	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	12.5 mg/1	500 TABLET in 1 BOTTLE (87063-014-05)
87063-014-10	87063-014	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	12.5 mg/1	10 TABLET in 1 BOTTLE (87063-014-10)
87063-014-20	87063-014	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	12.5 mg/1	20 TABLET in 1 BOTTLE (87063-014-20)
87063-014-30	87063-014	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (87063-014-30)
87063-014-60	87063-014	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	12.5 mg/1	60 TABLET in 1 BOTTLE (87063-014-60)
87063-014-90	87063-014	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	12.5 mg/1	90 TABLET in 1 BOTTLE (87063-014-90)