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=ANDA203277"
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
31722-753-06 31722-753 HUMAN PRESCRIPTION DRUG Lamivudine Lamivudine TABLET, FILM COATED ORAL 20140106 N/A ANDA ANDA203277 Camber Pharmaceuticals, Inc. LAMIVUDINE 150 mg/1 600 TABLET, FILM COATED in 1 BOTTLE (31722-753-06)
31722-753-31 31722-753 HUMAN PRESCRIPTION DRUG Lamivudine Lamivudine TABLET, FILM COATED ORAL 20140106 N/A ANDA ANDA203277 Camber Pharmaceuticals, Inc. LAMIVUDINE 150 mg/1 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-753-31)
31722-753-32 31722-753 HUMAN PRESCRIPTION DRUG Lamivudine Lamivudine TABLET, FILM COATED ORAL 20140106 N/A ANDA ANDA203277 Camber Pharmaceuticals, Inc. LAMIVUDINE 150 mg/1 100 TABLET, FILM COATED in 1 CARTON (31722-753-32)
31722-753-60 31722-753 HUMAN PRESCRIPTION DRUG Lamivudine Lamivudine TABLET, FILM COATED ORAL 20140106 N/A ANDA ANDA203277 Camber Pharmaceuticals, Inc. LAMIVUDINE 150 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (31722-753-60)
31722-754-06 31722-754 HUMAN PRESCRIPTION DRUG Lamivudine Lamivudine TABLET, FILM COATED ORAL 20140106 N/A ANDA ANDA203277 Camber Pharmaceuticals, Inc. LAMIVUDINE 300 mg/1 600 TABLET, FILM COATED in 1 BOTTLE (31722-754-06)
31722-754-30 31722-754 HUMAN PRESCRIPTION DRUG Lamivudine Lamivudine TABLET, FILM COATED ORAL 20140106 N/A ANDA ANDA203277 Camber Pharmaceuticals, Inc. LAMIVUDINE 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-754-30)
31722-754-31 31722-754 HUMAN PRESCRIPTION DRUG Lamivudine Lamivudine TABLET, FILM COATED ORAL 20140106 N/A ANDA ANDA203277 Camber Pharmaceuticals, Inc. LAMIVUDINE 300 mg/1 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-754-31)
31722-754-32 31722-754 HUMAN PRESCRIPTION DRUG Lamivudine Lamivudine TABLET, FILM COATED ORAL 20140106 N/A ANDA ANDA203277 Camber Pharmaceuticals, Inc. LAMIVUDINE 300 mg/1 100 TABLET, FILM COATED in 1 CARTON (31722-754-32)
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