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
68071-3924-3	68071-3924	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20251204	N/A	ANDA	ANDA072215	NuCare Pharamceuticals, Inc.	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (68071-3924-3)
50228-232-01	50228-232	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20250212	N/A	ANDA	ANDA072215	ScieGen Pharmaceuticals, Inc.	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (50228-232-01)
50228-232-05	50228-232	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20250212	N/A	ANDA	ANDA072215	ScieGen Pharmaceuticals, Inc.	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE (50228-232-05)
50228-233-01	50228-233	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20250212	N/A	ANDA	ANDA072215	ScieGen Pharmaceuticals, Inc.	METOCLOPRAMIDE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (50228-233-01)
50228-233-05	50228-233	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20250212	N/A	ANDA	ANDA072215	ScieGen Pharmaceuticals, Inc.	METOCLOPRAMIDE HYDROCHLORIDE	10 mg/1	500 TABLET in 1 BOTTLE (50228-233-05)
50228-233-10	50228-233	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20250212	N/A	ANDA	ANDA072215	ScieGen Pharmaceuticals, Inc.	METOCLOPRAMIDE HYDROCHLORIDE	10 mg/1	1000 TABLET in 1 BOTTLE (50228-233-10)