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
59762-2010-1	59762-2010	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20190624	N/A	NDA AUTHORIZED GENERIC	NDA019787	Greenstone LLC	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE (59762-2010-1)
59762-2010-3	59762-2010	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20190624	N/A	NDA AUTHORIZED GENERIC	NDA019787	Greenstone LLC	AMLODIPINE BESYLATE	5 mg/1	300 TABLET in 1 BOTTLE (59762-2010-3)
59762-2010-9	59762-2010	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20190624	N/A	NDA AUTHORIZED GENERIC	NDA019787	Greenstone LLC	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (59762-2010-9)
59762-2135-1	59762-2135	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20191113	N/A	NDA AUTHORIZED GENERIC	NDA019787	Greenstone LLC	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE (59762-2135-1)
59762-2135-9	59762-2135	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20190624	N/A	NDA AUTHORIZED GENERIC	NDA019787	Greenstone LLC	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (59762-2135-9)
59762-2242-3	59762-2242	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20190624	N/A	NDA AUTHORIZED GENERIC	NDA019787	Greenstone LLC	AMLODIPINE BESYLATE	2.5 mg/1	300 TABLET in 1 BOTTLE (59762-2242-3)
59762-2242-9	59762-2242	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20190624	N/A	NDA AUTHORIZED GENERIC	NDA019787	Greenstone LLC	AMLODIPINE BESYLATE	2.5 mg/1	90 TABLET in 1 BOTTLE (59762-2242-9)
71610-469-60	71610-469	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20221017	N/A	NDA AUTHORIZED GENERIC	NDA019787	Aphena Pharma Solutions - Tennessee, LLC	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (71610-469-60)
58151-355-88	58151-355	HUMAN PRESCRIPTION DRUG	Norvasc	amlodipine besylate	TABLET	ORAL	20240209	N/A	NDA	NDA019787	Viatris Specialty LLC	AMLODIPINE BESYLATE	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (58151-355-88) / 1 TABLET in 1 BLISTER PACK
0069-1520-68	0069-1520	HUMAN PRESCRIPTION DRUG	Norvasc	amlodipine besylate	TABLET	ORAL	19920731	N/A	NDA	NDA019787	PFIZER LABORATORIES DIV PFIZER INC	AMLODIPINE BESYLATE	2.5 mg/1	90 TABLET in 1 BOTTLE (0069-1520-68)
0069-1530-41	0069-1530	HUMAN PRESCRIPTION DRUG	Norvasc	amlodipine besylate	TABLET	ORAL	19920731	N/A	NDA	NDA019787	PFIZER LABORATORIES DIV PFIZER INC	AMLODIPINE BESYLATE	5 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (0069-1530-41) / 1 TABLET in 1 BLISTER PACK
0069-1530-68	0069-1530	HUMAN PRESCRIPTION DRUG	Norvasc	amlodipine besylate	TABLET	ORAL	19920731	N/A	NDA	NDA019787	PFIZER LABORATORIES DIV PFIZER INC	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (0069-1530-68)
0069-1530-72	0069-1530	HUMAN PRESCRIPTION DRUG	Norvasc	amlodipine besylate	TABLET	ORAL	19920731	N/A	NDA	NDA019787	PFIZER LABORATORIES DIV PFIZER INC	AMLODIPINE BESYLATE	5 mg/1	300 TABLET in 1 BOTTLE (0069-1530-72)
0069-1540-41	0069-1540	HUMAN PRESCRIPTION DRUG	Norvasc	amlodipine besylate	TABLET	ORAL	19920731	20250228	NDA	NDA019787	PFIZER LABORATORIES DIV PFIZER INC	AMLODIPINE BESYLATE	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (0069-1540-41) / 1 TABLET in 1 BLISTER PACK
0069-1540-68	0069-1540	HUMAN PRESCRIPTION DRUG	Norvasc	amlodipine besylate	TABLET	ORAL	19920731	N/A	NDA	NDA019787	PFIZER LABORATORIES DIV PFIZER INC	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (0069-1540-68)
71610-469-53	71610-469	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20221017	N/A	NDA AUTHORIZED GENERIC	NDA019787	Aphena Pharma Solutions - Tennessee, LLC	AMLODIPINE BESYLATE	10 mg/1	60 TABLET in 1 BOTTLE (71610-469-53)
71610-469-45	71610-469	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20200929	N/A	NDA AUTHORIZED GENERIC	NDA019787	Aphena Pharma Solutions - Tennessee, LLC	AMLODIPINE BESYLATE	10 mg/1	45 TABLET in 1 BOTTLE (71610-469-45)
71610-469-30	71610-469	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20200929	N/A	NDA AUTHORIZED GENERIC	NDA019787	Aphena Pharma Solutions - Tennessee, LLC	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BOTTLE (71610-469-30)