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
71209-083-03	71209-083	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20180630	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71209-083-03)
71209-083-05	71209-083	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221124	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71209-083-05)
71209-083-10	71209-083	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221124	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71209-083-10)
71209-083-11	71209-083	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20180630	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (71209-083-11)
71209-084-03	71209-084	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20180630	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71209-084-03)
71209-084-05	71209-084	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221124	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71209-084-05)
71209-084-10	71209-084	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221124	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71209-084-10)
71209-084-11	71209-084	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20180630	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (71209-084-11)
71209-085-03	71209-085	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20180630	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71209-085-03)
71209-085-05	71209-085	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221124	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71209-085-05)
71209-085-10	71209-085	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20221124	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71209-085-10)
71209-085-11	71209-085	HUMAN PRESCRIPTION DRUG	Labetalol Hydrochloride	Labetalol Hydrochloride	TABLET, FILM COATED	ORAL	20180630	N/A	ANDA	ANDA211325	Cadila Pharmaceuticals Limited	LABETALOL HYDROCHLORIDE	300 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (71209-085-11)