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=ANDA208303"
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
68382-624-31 68382-624 HUMAN PRESCRIPTION DRUG Roflumilast Roflumilast TABLET ORAL 20230518 N/A ANDA ANDA208303 Zydus Pharmaceuticals USA Inc. ROFLUMILAST 250 ug/1 1 BLISTER PACK in 1 CARTON (68382-624-31) / 28 TABLET in 1 BLISTER PACK
68382-624-83 68382-624 HUMAN PRESCRIPTION DRUG Roflumilast Roflumilast TABLET ORAL 20230518 N/A ANDA ANDA208303 Zydus Pharmaceuticals USA Inc. ROFLUMILAST 250 ug/1 2 BLISTER PACK in 1 CARTON (68382-624-83) / 10 TABLET in 1 BLISTER PACK (68382-624-30)
70771-1674-3 70771-1674 HUMAN PRESCRIPTION DRUG Roflumilast Roflumilast TABLET ORAL 20221003 N/A ANDA ANDA208303 Zydus Lifesciences Limited ROFLUMILAST 500 ug/1 30 TABLET in 1 BOTTLE (70771-1674-3)
70771-1674-9 70771-1674 HUMAN PRESCRIPTION DRUG Roflumilast Roflumilast TABLET ORAL 20221003 N/A ANDA ANDA208303 Zydus Lifesciences Limited ROFLUMILAST 500 ug/1 90 TABLET in 1 BOTTLE (70771-1674-9)
70771-1673-3 70771-1673 HUMAN PRESCRIPTION DRUG Roflumilast Roflumilast TABLET ORAL 20230518 N/A ANDA ANDA208303 Zydus Lifesciences Limited ROFLUMILAST 250 ug/1 2 BLISTER PACK in 1 CARTON (70771-1673-3) / 10 TABLET in 1 BLISTER PACK (70771-1673-2)
70771-1673-8 70771-1673 HUMAN PRESCRIPTION DRUG Roflumilast Roflumilast TABLET ORAL 20230518 N/A ANDA ANDA208303 Zydus Lifesciences Limited ROFLUMILAST 250 ug/1 1 BLISTER PACK in 1 CARTON (70771-1673-8) / 28 TABLET in 1 BLISTER PACK
68382-969-06 68382-969 HUMAN PRESCRIPTION DRUG Roflumilast Roflumilast TABLET ORAL 20221003 N/A ANDA ANDA208303 Zydus Pharmaceuticals USA Inc. ROFLUMILAST 500 ug/1 30 TABLET in 1 BOTTLE (68382-969-06)
68382-969-16 68382-969 HUMAN PRESCRIPTION DRUG Roflumilast Roflumilast TABLET ORAL 20221003 N/A ANDA ANDA208303 Zydus Pharmaceuticals USA Inc. ROFLUMILAST 500 ug/1 90 TABLET in 1 BOTTLE (68382-969-16)
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