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=ANDA213808"
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
70748-196-07 70748-196 HUMAN PRESCRIPTION DRUG sacubitril and valsartan sacubitril and valsartan TABLET, FILM COATED ORAL 20250729 N/A ANDA ANDA213808 Lupin Pharmaceuticals, Inc. SACUBITRIL; VALSARTAN 49 mg/1; 51 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (70748-196-07)
70748-197-07 70748-197 HUMAN PRESCRIPTION DRUG sacubitril and valsartan sacubitril and valsartan TABLET, FILM COATED ORAL 20250729 N/A ANDA ANDA213808 Lupin Pharmaceuticals, Inc. SACUBITRIL; VALSARTAN 97 mg/1; 103 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (70748-197-07)
70748-195-07 70748-195 HUMAN PRESCRIPTION DRUG sacubitril and valsartan sacubitril and valsartan TABLET, FILM COATED ORAL 20250729 N/A ANDA ANDA213808 Lupin Pharmaceuticals, Inc. SACUBITRIL; VALSARTAN 24 mg/1; 26 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (70748-195-07)
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