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)
检索条件:" 注册申请号=ANDA090682"
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
53002-0061-3 53002-0061 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 10 TABLET, FILM COATED in 1 BOTTLE (53002-0061-3)
68071-2738-1 68071-2738 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20220527 N/A ANDA ANDA090682 NuCare Pharmaceuticals,Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68071-2738-1)
68071-2738-4 68071-2738 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20220527 N/A ANDA ANDA090682 NuCare Pharmaceuticals,Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68071-2738-4)
51655-703-04 51655-703 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20230815 N/A ANDA ANDA090682 Northwind Pharmaceuticals, LLC VALACYCLOVIR HYDROCHLORIDE 1 g/1 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-04)
51655-703-21 51655-703 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20230403 N/A ANDA ANDA090682 Northwind Pharmaceuticals, LLC VALACYCLOVIR HYDROCHLORIDE 1 g/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-21)
51655-703-53 51655-703 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20230615 N/A ANDA ANDA090682 Northwind Pharmaceuticals, LLC VALACYCLOVIR HYDROCHLORIDE 1 g/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-53)
68071-2749-3 68071-2749 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20220602 N/A ANDA ANDA090682 NuCare Pharmaceuticals,Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-2749-3)
51655-633-84 51655-633 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA090682 Northwind Pharmaceuticals, LLC VALACYCLOVIR HYDROCHLORIDE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-633-84)
51655-633-21 51655-633 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20230531 N/A ANDA ANDA090682 Northwind Pharmaceuticals, LLC VALACYCLOVIR HYDROCHLORIDE 500 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-633-21)
76420-053-12 76420-053 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20201024 N/A ANDA ANDA090682 Asclemed USA, Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (76420-053-12)
76420-053-30 76420-053 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20201024 N/A ANDA ANDA090682 Asclemed USA, Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-053-30)
50090-5852-0 50090-5852 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA090682 A-S Medication Solutions VALACYCLOVIR HYDROCHLORIDE 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-5852-0)
50090-5852-2 50090-5852 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA090682 A-S Medication Solutions VALACYCLOVIR HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5852-2)
50090-5852-3 50090-5852 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA090682 A-S Medication Solutions VALACYCLOVIR HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5852-3)
50090-5852-1 50090-5852 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA090682 A-S Medication Solutions VALACYCLOVIR HYDROCHLORIDE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (50090-5852-1)
68071-2921-9 68071-2921 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20230125 N/A ANDA ANDA090682 NuCare Pharmaceuticals,Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-2921-9)
53002-7830-6 53002-7830 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (53002-7830-6)
63739-525-10 63739-525 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20100524 N/A ANDA ANDA090682 Mckesson Corporation DBA SKY Packaginng VALACYCLOVIR HYDROCHLORIDE 500 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-525-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
53002-7830-1 53002-7830 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (53002-7830-1)
53002-7830-2 53002-7830 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (53002-7830-2)
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