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=ANDA078629"
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
0143-9744-10 0143-9744 HUMAN PRESCRIPTION DRUG Granisetron Hydrochloride Granisetron Hydrochloride INJECTION INTRAVENOUS 20091223 N/A ANDA ANDA078629 Hikma Pharmaceuticals USA Inc. GRANISETRON HYDROCHLORIDE 1 mg/mL 10 VIAL, SINGLE-USE in 1 PACKAGE (0143-9744-10) / 1 mL in 1 VIAL, SINGLE-USE (0143-9744-01)
0143-9745-05 0143-9745 HUMAN PRESCRIPTION DRUG Granisetron Hydrochloride Granisetron Hydrochloride INJECTION INTRAVENOUS 20091223 N/A ANDA ANDA078629 Hikma Pharmaceuticals USA Inc. GRANISETRON HYDROCHLORIDE 1 mg/mL 5 VIAL, MULTI-DOSE in 1 CARTON (0143-9745-05) / 4 mL in 1 VIAL, MULTI-DOSE (0143-9745-01)
0143-9745-10 0143-9745 HUMAN PRESCRIPTION DRUG Granisetron Hydrochloride Granisetron Hydrochloride INJECTION INTRAVENOUS 20091223 N/A ANDA ANDA078629 Hikma Pharmaceuticals USA Inc. GRANISETRON HYDROCHLORIDE 1 mg/mL 10 VIAL, MULTI-DOSE in 1 CARTON (0143-9745-10) / 4 mL in 1 VIAL, MULTI-DOSE (0143-9745-01)
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