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
87063-016-60	87063-016	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	50 mg/1	60 TABLET in 1 BOTTLE (87063-016-60)
87063-016-90	87063-016	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20251017	N/A	ANDA	ANDA040596	ASCLEMED USA INC.	PROMETHAZINE HYDROCHLORIDE	50 mg/1	90 TABLET in 1 BOTTLE (87063-016-90)
76420-692-01	76420-692	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20240226	N/A	ANDA	ANDA040596	Asclemed USA, Inc.	PROMETHAZINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (76420-692-01)
76420-692-30	76420-692	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20240226	N/A	ANDA	ANDA040596	Asclemed USA, Inc.	PROMETHAZINE HYDROCHLORIDE	50 mg/1	30 TABLET in 1 BOTTLE (76420-692-30)
76420-692-60	76420-692	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20240226	N/A	ANDA	ANDA040596	Asclemed USA, Inc.	PROMETHAZINE HYDROCHLORIDE	50 mg/1	60 TABLET in 1 BOTTLE (76420-692-60)
76420-692-90	76420-692	HUMAN PRESCRIPTION DRUG	Promethazine Hydrochloride	Promethazine Hydrochloride	TABLET	ORAL	20240226	N/A	ANDA	ANDA040596	Asclemed USA, Inc.	PROMETHAZINE HYDROCHLORIDE	50 mg/1	90 TABLET in 1 BOTTLE (76420-692-90)
72189-176-20	72189-176	HUMAN PRESCRIPTION DRUG	PROMETHAZINE HYDROCHLORIDE	PROMETHAZINE HYDROCHLORIDE	TABLET	ORAL	20210209	N/A	ANDA	ANDA040596	DIRECT RX	PROMETHAZINE HYDROCHLORIDE	25 mg/1	20 TABLET in 1 BOTTLE (72189-176-20)
72189-176-30	72189-176	HUMAN PRESCRIPTION DRUG	PROMETHAZINE HYDROCHLORIDE	PROMETHAZINE HYDROCHLORIDE	TABLET	ORAL	20210209	N/A	ANDA	ANDA040596	DIRECT RX	PROMETHAZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (72189-176-30)