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=ANDA090404"
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
68382-319-77 68382-319 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20110131 N/A ANDA ANDA090404 Zydus Pharmaceuticals USA Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 100 BLISTER PACK in 1 CARTON (68382-319-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-319-30)
68382-319-10 68382-319 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20110131 N/A ANDA ANDA090404 Zydus Pharmaceuticals USA Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-319-10)
68382-319-05 68382-319 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20110131 N/A ANDA ANDA090404 Zydus Pharmaceuticals USA Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-319-05)
68382-319-01 68382-319 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20110131 N/A ANDA ANDA090404 Zydus Pharmaceuticals USA Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-319-01)
65841-754-01 65841-754 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20110131 N/A ANDA ANDA090404 Zydus Lifesciences Limited TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-754-01)
65841-754-05 65841-754 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20110131 N/A ANDA ANDA090404 Zydus Lifesciences Limited TRAMADOL HYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-754-05)
65841-754-10 65841-754 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20110131 N/A ANDA ANDA090404 Zydus Lifesciences Limited TRAMADOL HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-754-10)
65841-754-30 65841-754 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20110131 N/A ANDA ANDA090404 Zydus Lifesciences Limited TRAMADOL HYDROCHLORIDE 50 mg/1 10 BLISTER PACK in 1 CARTON (65841-754-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
71205-066-15 71205-066 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090404 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71205-066-15)
71205-066-60 71205-066 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090404 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-066-60)
71205-066-72 71205-066 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090404 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71205-066-72)
71205-066-78 71205-066 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090404 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71205-066-78)
71205-066-90 71205-066 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090404 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-066-90)
71205-066-20 71205-066 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090404 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-066-20)
71205-066-30 71205-066 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090404 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-066-30)
71205-066-40 71205-066 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA090404 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71205-066-40)
61919-597-20 61919-597 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20200723 N/A ANDA ANDA090404 DirectRX TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (61919-597-20)
61919-597-72 61919-597 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20200723 N/A ANDA ANDA090404 DirectRX TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (61919-597-72)
61919-597-82 61919-597 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20200723 N/A ANDA ANDA090404 DirectRX TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (61919-597-82)
61919-597-84 61919-597 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, FILM COATED ORAL 20200723 N/A ANDA ANDA090404 DirectRX TRAMADOL HYDROCHLORIDE 50 mg/1 240 TABLET, FILM COATED in 1 BOTTLE (61919-597-84)
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