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
70518-2518-1	70518-2518	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20200706	N/A	ANDA	ANDA203834	REMEDYREPACK INC.	ACYCLOVIR	800 mg/1	30 TABLET in 1 BLISTER PACK (70518-2518-1)
70518-2518-2	70518-2518	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20230412	N/A	ANDA	ANDA203834	REMEDYREPACK INC.	ACYCLOVIR	800 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (70518-2518-2)
31722-778-01	31722-778	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20131129	N/A	ANDA	ANDA203834	Camber Pharmaceuticals, Inc.	ACYCLOVIR	800 mg/1	100 TABLET in 1 BOTTLE (31722-778-01)
31722-778-05	31722-778	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20131129	N/A	ANDA	ANDA203834	Camber Pharmaceuticals, Inc.	ACYCLOVIR	800 mg/1	500 TABLET in 1 BOTTLE (31722-778-05)
70518-2117-0	70518-2117	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20190528	N/A	ANDA	ANDA203834	REMEDYREPACK INC.	ACYCLOVIR	400 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-2117-0)
70518-2117-2	70518-2117	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20200710	N/A	ANDA	ANDA203834	REMEDYREPACK INC.	ACYCLOVIR	400 mg/1	30 TABLET in 1 BLISTER PACK (70518-2117-2)
50090-6844-0	50090-6844	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20231129	N/A	ANDA	ANDA203834	A-S Medication Solutions	ACYCLOVIR	400 mg/1	90 TABLET in 1 BOTTLE (50090-6844-0)
51655-300-84	51655-300	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20230125	N/A	ANDA	ANDA203834	Northwind Health Company, LLC	ACYCLOVIR	400 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (51655-300-84)
68071-3222-3	68071-3222	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20170608	N/A	ANDA	ANDA203834	NuCare Pharmaceuticals, Inc.	ACYCLOVIR	800 mg/1	30 TABLET in 1 BOTTLE (68071-3222-3)
68071-3222-4	68071-3222	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20170608	N/A	ANDA	ANDA203834	NuCare Pharmaceuticals, Inc.	ACYCLOVIR	800 mg/1	14 TABLET in 1 BOTTLE (68071-3222-4)
68071-3222-5	68071-3222	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20170608	N/A	ANDA	ANDA203834	NuCare Pharmaceuticals, Inc.	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE (68071-3222-5)
68071-3222-7	68071-3222	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20170608	N/A	ANDA	ANDA203834	NuCare Pharmaceuticals, Inc.	ACYCLOVIR	800 mg/1	15 TABLET in 1 BOTTLE (68071-3222-7)
68071-4799-6	68071-4799	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20190312	N/A	ANDA	ANDA203834	NuCare Pharmaceuticals,Inc.	ACYCLOVIR	400 mg/1	60 TABLET in 1 BOTTLE (68071-4799-6)
60760-778-35	60760-778	HUMAN PRESCRIPTION DRUG	Acyclovir	Acyclovir	TABLET	ORAL	20240315	N/A	ANDA	ANDA203834	ST. MARY'S MEDICAL PARK PHARMACY	ACYCLOVIR	800 mg/1	35 TABLET in 1 BOTTLE, PLASTIC (60760-778-35)