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=ANDA074769"
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
0904-6560-61 0904-6560 HUMAN PRESCRIPTION DRUG Morphine Sulfate Extended Release Morphine Sulfate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110114 N/A ANDA ANDA074769 Major Pharmaceuticals MORPHINE SULFATE 100 mg/1 100 BLISTER PACK in 1 CARTON (0904-6560-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
63629-8505-1 63629-8505 HUMAN PRESCRIPTION DRUG Morphine Sulfate Extended Release Morphine Sulfate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240404 N/A ANDA ANDA074769 Bryant Ranch Prepack MORPHINE SULFATE 200 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-8505-1)
72162-1352-1 72162-1352 HUMAN PRESCRIPTION DRUG Morphine Sulfate Extended Release Morphine Sulfate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240207 N/A ANDA ANDA074769 Bryant Ranch Prepack MORPHINE SULFATE 200 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1352-1)
42858-805-01 42858-805 HUMAN PRESCRIPTION DRUG Morphine Sulfate Extended Release Morphine Sulfate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110114 N/A ANDA ANDA074769 Rhodes Pharmaceuticals L. P. MORPHINE SULFATE 200 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42858-805-01)
42858-804-01 42858-804 HUMAN PRESCRIPTION DRUG Morphine Sulfate Extended Release Morphine Sulfate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110114 N/A ANDA ANDA074769 Rhodes Pharmaceuticals L. P. MORPHINE SULFATE 100 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42858-804-01)
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