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=ANDA091534"
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
68382-423-06 68382-423 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride INJECTION INTRAMUSCULAR; INTRAVENOUS 20130301 N/A ANDA ANDA091534 Zydus Pharmaceuticals USA Inc. RANITIDINE HYDROCHLORIDE 25 mg/mL 6 mL in 1 VIAL, MULTI-DOSE (68382-423-06)
68382-422-02 68382-422 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride INJECTION INTRAMUSCULAR; INTRAVENOUS 20130301 N/A ANDA ANDA091534 Zydus Pharmaceuticals USA Inc. RANITIDINE HYDROCHLORIDE 25 mg/mL 10 VIAL in 1 CARTON (68382-422-02) / 2 mL in 1 VIAL
70710-1550-1 70710-1550 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20190221 N/A ANDA ANDA091534 Zydus Pharmaceuticals USA Inc. RANITIDINE HYDROCHLORIDE 25 mg/mL 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70710-1550-1) / 40 mL in 1 VIAL, PHARMACY BULK PACKAGE
65841-763-02 65841-763 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride INJECTION INTRAMUSCULAR; INTRAVENOUS 20130301 N/A ANDA ANDA091534 Zydus Lifesciences Limited RANITIDINE HYDROCHLORIDE 25 mg/mL 10 VIAL in 1 CARTON (65841-763-02) / 2 mL in 1 VIAL
72785-0001-1 72785-0001 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride ranitidine hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20190221 N/A ANDA ANDA091534 Zydus Lifesciences Limited RANITIDINE HYDROCHLORIDE 25 mg/mL 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (72785-0001-1) / 40 mL in 1 VIAL, PHARMACY BULK PACKAGE
65841-764-06 65841-764 HUMAN PRESCRIPTION DRUG Ranitidine Hydrochloride Ranitidine Hydrochloride INJECTION INTRAMUSCULAR; INTRAVENOUS 20130301 N/A ANDA ANDA091534 Zydus Lifesciences Limited RANITIDINE HYDROCHLORIDE 25 mg/mL 6 mL in 1 VIAL, MULTI-DOSE (65841-764-06)
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