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
29300-252-01	29300-252	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221001	N/A	ANDA	ANDA212719	Unichem Pharmaceuticals (USA), Inc.	LABETALOL HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (29300-252-01)
29300-252-05	29300-252	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221001	N/A	ANDA	ANDA212719	Unichem Pharmaceuticals (USA), Inc.	LABETALOL HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (29300-252-05)
29300-253-01	29300-253	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221001	N/A	ANDA	ANDA212719	Unichem Pharmaceuticals (USA), Inc.	LABETALOL HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (29300-253-01)
29300-253-05	29300-253	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221001	N/A	ANDA	ANDA212719	Unichem Pharmaceuticals (USA), Inc.	LABETALOL HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (29300-253-05)
29300-254-01	29300-254	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221001	N/A	ANDA	ANDA212719	Unichem Pharmaceuticals (USA), Inc.	LABETALOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (29300-254-01)
29300-254-05	29300-254	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221001	N/A	ANDA	ANDA212719	Unichem Pharmaceuticals (USA), Inc.	LABETALOL HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (29300-254-05)