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=ANDA210401"
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
71335-3103-3 71335-3103 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20260316 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 30 TABLET in 1 BOTTLE (71335-3103-3)
71335-3103-4 71335-3103 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20260316 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 50 TABLET in 1 BOTTLE (71335-3103-4)
71335-3103-5 71335-3103 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20260316 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 15 TABLET in 1 BOTTLE (71335-3103-5)
71335-3103-6 71335-3103 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20260316 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 60 TABLET in 1 BOTTLE (71335-3103-6)
71335-3103-7 71335-3103 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20260316 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 25 TABLET in 1 BOTTLE (71335-3103-7)
71335-3103-8 71335-3103 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20260316 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 10 TABLET in 1 BOTTLE (71335-3103-8)
71335-3103-9 71335-3103 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20260316 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 40 TABLET in 1 BOTTLE (71335-3103-9)
71335-1222-5 71335-1222 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20190506 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 800 mg/1 50 TABLET in 1 BOTTLE (71335-1222-5)
71335-1222-6 71335-1222 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20250130 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 800 mg/1 10 TABLET in 1 BOTTLE (71335-1222-6)
71335-1222-7 71335-1222 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20190523 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 800 mg/1 40 TABLET in 1 BOTTLE (71335-1222-7)
71335-1222-8 71335-1222 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20250130 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 800 mg/1 21 TABLET in 1 BOTTLE (71335-1222-8)
71335-1222-9 71335-1222 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20250130 N/A ANDA ANDA210401 Bryant Ranch Prepack ACYCLOVIR 800 mg/1 90 TABLET in 1 BOTTLE (71335-1222-9)
67296-2162-2 67296-2162 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20230620 N/A ANDA ANDA210401 Redpharm Drug ACYCLOVIR 400 mg/1 20 TABLET in 1 BOTTLE (67296-2162-2)
69117-0018-1 69117-0018 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20180504 N/A ANDA ANDA210401 YILING PHARMACEUTICAL, INC. ACYCLOVIR 400 mg/1 100 TABLET in 1 BOTTLE (69117-0018-1)
69117-0018-2 69117-0018 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20180504 N/A ANDA ANDA210401 YILING PHARMACEUTICAL, INC. ACYCLOVIR 400 mg/1 500 TABLET in 1 BOTTLE (69117-0018-2)
50090-6578-0 50090-6578 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20230804 N/A ANDA ANDA210401 A-S Medication Solutions ACYCLOVIR 800 mg/1 35 TABLET in 1 BOTTLE (50090-6578-0)
50090-6578-2 50090-6578 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20230804 N/A ANDA ANDA210401 A-S Medication Solutions ACYCLOVIR 800 mg/1 70 TABLET in 1 BOTTLE (50090-6578-2)
68788-8724-1 68788-8724 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20240816 N/A ANDA ANDA210401 Preferred Pharmaceuticals Inc ACYCLOVIR 400 mg/1 100 TABLET in 1 BOTTLE (68788-8724-1)
68788-8724-2 68788-8724 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20240816 N/A ANDA ANDA210401 Preferred Pharmaceuticals Inc ACYCLOVIR 400 mg/1 21 TABLET in 1 BOTTLE (68788-8724-2)
68788-8724-3 68788-8724 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20240816 N/A ANDA ANDA210401 Preferred Pharmaceuticals Inc ACYCLOVIR 400 mg/1 30 TABLET in 1 BOTTLE (68788-8724-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase