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
70771-1521-3	70771-1521	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1521-3)
70771-1521-7	70771-1521	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	25 mg/1	3 BLISTER PACK in 1 CARTON (70771-1521-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1521-2)
70771-1521-9	70771-1521	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1521-9)
70771-1522-3	70771-1522	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1522-3)
70771-1522-7	70771-1522	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	100 mg/1	3 BLISTER PACK in 1 CARTON (70771-1522-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1522-2)
70771-1522-9	70771-1522	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1522-9)
70771-1523-3	70771-1523	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1523-3)
70771-1523-7	70771-1523	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	150 mg/1	3 BLISTER PACK in 1 CARTON (70771-1523-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1523-2)
70771-1523-9	70771-1523	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA213065	Cadila Healthcare Limited	ERLOTINIB HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1523-9)
68382-913-06	68382-913	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (68382-913-06)
68382-913-16	68382-913	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (68382-913-16)
68382-913-84	68382-913	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	25 mg/1	3 BLISTER PACK in 1 CARTON (68382-913-84) / 10 TABLET in 1 BLISTER PACK (68382-913-30)
68382-914-06	68382-914	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	100 mg/1	30 TABLET in 1 BOTTLE (68382-914-06)
68382-914-16	68382-914	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	100 mg/1	90 TABLET in 1 BOTTLE (68382-914-16)
68382-914-84	68382-914	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	100 mg/1	3 BLISTER PACK in 1 CARTON (68382-914-84) / 10 TABLET in 1 BLISTER PACK (68382-914-30)
68382-915-06	68382-915	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	150 mg/1	30 TABLET in 1 BOTTLE (68382-915-06)
68382-915-16	68382-915	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	150 mg/1	90 TABLET in 1 BOTTLE (68382-915-16)
68382-915-84	68382-915	HUMAN PRESCRIPTION DRUG	Erlotinib	Erlotinib	TABLET	ORAL	20200430	N/A	ANDA	ANDA213065	Zydus Pharmaceuticals USA Inc.	ERLOTINIB HYDROCHLORIDE	150 mg/1	3 BLISTER PACK in 1 CARTON (68382-915-84) / 10 TABLET in 1 BLISTER PACK (68382-915-30)