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=ANDA040362"
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
51655-208-52 51655-208 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20220511 20260501 ANDA ANDA040362 Northwind Health Company, LLC PREDNISONE 20 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-208-52)
51655-208-53 51655-208 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20220926 20260501 ANDA ANDA040362 Northwind Health Company, LLC PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (51655-208-53)
50090-5202-0 50090-5202 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20201002 N/A ANDA ANDA040362 A-S Medication Solutions PREDNISONE 10 mg/1 60 TABLET in 1 BOTTLE (50090-5202-0)
50090-5202-1 50090-5202 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20201002 N/A ANDA ANDA040362 A-S Medication Solutions PREDNISONE 10 mg/1 20 TABLET in 1 BOTTLE (50090-5202-1)
51655-208-18 51655-208 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20220621 20260501 ANDA ANDA040362 Northwind Health Company, LLC PREDNISONE 20 mg/1 18 TABLET in 1 BOTTLE, PLASTIC (51655-208-18)
51655-208-54 51655-208 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20221130 20260501 ANDA ANDA040362 Northwind Health Company, LLC PREDNISONE 20 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (51655-208-54)
51655-208-55 51655-208 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20221130 20260501 ANDA ANDA040362 Northwind Health Company, LLC PREDNISONE 20 mg/1 5 TABLET in 1 BOTTLE, PLASTIC (51655-208-55)
51655-208-87 51655-208 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230912 20260501 ANDA ANDA040362 Northwind Health Company, LLC PREDNISONE 20 mg/1 6 TABLET in 1 BOTTLE, PLASTIC (51655-208-87)
60760-255-21 60760-255 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180213 N/A ANDA ANDA040362 St. Mary’s Medical Park Pharmacy PREDNISONE 5 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (60760-255-21)
51655-416-54 51655-416 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20220621 20260501 ANDA ANDA040362 Northwind Health Company, LLC PREDNISONE 10 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (51655-416-54)
60760-179-18 60760-179 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230809 N/A ANDA ANDA040362 St. Mary's Medical Park Pharmacy PREDNISONE 10 mg/1 18 TABLET in 1 BOTTLE, PLASTIC (60760-179-18)
51655-416-21 51655-416 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20210804 20260501 ANDA ANDA040362 Northwind Health Company, LLC PREDNISONE 10 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (51655-416-21)
63187-020-30 63187-020 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180904 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 5 mg/1 30 TABLET in 1 BOTTLE (63187-020-30)
63187-020-36 63187-020 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180904 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 5 mg/1 36 TABLET in 1 BOTTLE (63187-020-36)
63187-020-15 63187-020 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180904 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 5 mg/1 15 TABLET in 1 BOTTLE (63187-020-15)
63187-020-21 63187-020 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180904 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 5 mg/1 21 TABLET in 1 BOTTLE (63187-020-21)
63187-020-10 63187-020 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180904 N/A ANDA ANDA040362 Proficient Rx LP PREDNISONE 5 mg/1 10 TABLET in 1 BOTTLE (63187-020-10)
66267-171-20 66267-171 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180118 N/A ANDA ANDA040362 NuCare Pharmaceuticals,Inc. PREDNISONE 10 mg/1 20 TABLET in 1 BOTTLE (66267-171-20)
66267-171-40 66267-171 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180118 N/A ANDA ANDA040362 NuCare Pharmaceuticals,Inc. PREDNISONE 10 mg/1 40 TABLET in 1 BOTTLE (66267-171-40)
66267-172-06 66267-172 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180118 N/A ANDA ANDA040362 NuCare Pharmaceuticals,Inc. PREDNISONE 5 mg/1 6 TABLET in 1 BOTTLE (66267-172-06)
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