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
50090-7466-0	50090-7466	HUMAN PRESCRIPTION DRUG	CLOPIDOGREL	CLOPIDOGREL BISULFATE	TABLET	ORAL	20241202	N/A	ANDA	ANDA203632	A-S Medication Solutions	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET in 1 BOTTLE (50090-7466-0)
50090-7466-1	50090-7466	HUMAN PRESCRIPTION DRUG	CLOPIDOGREL	CLOPIDOGREL BISULFATE	TABLET	ORAL	20241202	N/A	ANDA	ANDA203632	A-S Medication Solutions	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET in 1 BOTTLE (50090-7466-1)
70518-4373-0	70518-4373	HUMAN PRESCRIPTION DRUG	CLOPIDOGREL	CLOPIDOGREL BISULFATE	TABLET	ORAL	20250626	N/A	ANDA	ANDA203632	REMEDYREPACK INC.	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4373-0)
50090-7467-0	50090-7467	HUMAN PRESCRIPTION DRUG	CLOPIDOGREL	CLOPIDOGREL BISULFATE	TABLET	ORAL	20241202	N/A	ANDA	ANDA203632	A-S Medication Solutions	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET in 1 BOTTLE (50090-7467-0)
67877-276-05	67877-276	HUMAN PRESCRIPTION DRUG	CLOPIDOGREL	CLOPIDOGREL BISULFATE	TABLET	ORAL	20240516	N/A	ANDA	ANDA203632	Ascend Laboratories, LLC	CLOPIDOGREL BISULFATE	75 mg/1	500 TABLET in 1 BOTTLE (67877-276-05)
67877-276-30	67877-276	HUMAN PRESCRIPTION DRUG	CLOPIDOGREL	CLOPIDOGREL BISULFATE	TABLET	ORAL	20240516	N/A	ANDA	ANDA203632	Ascend Laboratories, LLC	CLOPIDOGREL BISULFATE	75 mg/1	30 TABLET in 1 BOTTLE (67877-276-30)
67877-276-90	67877-276	HUMAN PRESCRIPTION DRUG	CLOPIDOGREL	CLOPIDOGREL BISULFATE	TABLET	ORAL	20240516	N/A	ANDA	ANDA203632	Ascend Laboratories, LLC	CLOPIDOGREL BISULFATE	75 mg/1	90 TABLET in 1 BOTTLE (67877-276-90)