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=ANDA077316"
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
55154-5678-0 55154-5678 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20110218 N/A ANDA ANDA077316 Cardinal Health 107, LLC CARVEDILOL 6.25 mg/1 10 BLISTER PACK in 1 BAG (55154-5678-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-5677-0 55154-5677 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20110218 N/A ANDA ANDA077316 Cardinal Health 107, LLC CARVEDILOL 3.125 mg/1 10 BLISTER PACK in 1 BAG (55154-5677-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-5676-0 55154-5676 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20110218 N/A ANDA ANDA077316 Cardinal Health 107, LLC CARVEDILOL 25 mg/1 10 BLISTER PACK in 1 BAG (55154-5676-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-5675-0 55154-5675 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20110218 N/A ANDA ANDA077316 Cardinal Health 107, LLC CARVEDILOL 12.5 mg/1 10 BLISTER PACK in 1 BAG (55154-5675-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
51079-771-20 51079-771 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070914 N/A ANDA ANDA077316 Mylan Institutional Inc. CARVEDILOL 3.125 mg/1 100 BLISTER PACK in 1 CARTON (51079-771-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-771-01)
0378-3632-01 0378-3632 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070905 20250228 ANDA ANDA077316 Mylan Pharmaceuticals Inc. CARVEDILOL 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3632-01)
0378-3632-05 0378-3632 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070905 20250131 ANDA ANDA077316 Mylan Pharmaceuticals Inc. CARVEDILOL 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3632-05)
0378-3633-05 0378-3633 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070905 20250331 ANDA ANDA077316 Mylan Pharmaceuticals Inc. CARVEDILOL 12.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3633-05)
0378-3634-01 0378-3634 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070905 20241130 ANDA ANDA077316 Mylan Pharmaceuticals Inc. CARVEDILOL 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3634-01)
0378-3634-05 0378-3634 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070905 20250331 ANDA ANDA077316 Mylan Pharmaceuticals Inc. CARVEDILOL 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3634-05)
51079-930-20 51079-930 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070914 N/A ANDA ANDA077316 Mylan Institutional Inc. CARVEDILOL 6.25 mg/1 100 BLISTER PACK in 1 CARTON (51079-930-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-930-01)
51079-931-20 51079-931 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070914 N/A ANDA ANDA077316 Mylan Institutional Inc. CARVEDILOL 12.5 mg/1 100 BLISTER PACK in 1 CARTON (51079-931-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-931-01)
51079-932-20 51079-932 HUMAN PRESCRIPTION DRUG Carvedilol carvedilol TABLET, FILM COATED ORAL 20070914 N/A ANDA ANDA077316 Mylan Institutional Inc. CARVEDILOL 25 mg/1 100 BLISTER PACK in 1 CARTON (51079-932-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-932-01)
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