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=ANDA209882"
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
42385-947-18 42385-947 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20210720 N/A ANDA ANDA209882 Laurus Labs Limited METFORMIN HYDROCHLORIDE 500 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (42385-947-18)
42385-949-90 42385-949 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20220801 N/A ANDA ANDA209882 Laurus Labs Limited METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (42385-949-90)
68788-8756-9 68788-8756 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20241014 N/A ANDA ANDA209882 Preferred Pharmaceuticals Inc. METFORMIN HYDROCHLORIDE 850 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8756-9)
68071-3833-8 68071-3833 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250418 N/A ANDA ANDA209882 NuCare Pharmaceuticals,Inc. METFORMIN HYDROCHLORIDE 850 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-3833-8)
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