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=ANDA078539"
符合检索条件的记录共 244 条，共 13 页，当前第 5 页 ，可点击列名称排序
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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
76420-915-00 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-915-00)
76420-915-03 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (76420-915-03)
76420-915-05 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-915-05)
76420-915-10 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (76420-915-10)
76420-915-11 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 BLISTER PACK in 1 CARTON (76420-915-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
76420-915-30 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-915-30)
76420-915-33 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BLISTER PACK in 1 CARTON (76420-915-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
76420-915-60 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-915-60)
76420-915-90 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-915-90)
76420-917-01 76420-917 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 24 mg/1 1 BLISTER PACK in 1 CARTON (76420-917-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK
50090-4671-0 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (50090-4671-0)
50090-4671-1 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-4671-1)
50090-4671-2 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (50090-4671-2)
61919-565-30 61919-565 HUMAN PRESCRIPTION DRUG ONDANSETRON ONDANSETRON TABLET, FILM COATED ORAL 20190822 N/A ANDA ANDA078539 Direct_Rx ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (61919-565-30)
61919-565-45 61919-565 HUMAN PRESCRIPTION DRUG ONDANSETRON ONDANSETRON TABLET, FILM COATED ORAL 20190822 N/A ANDA ANDA078539 Direct_Rx ONDANSETRON HYDROCHLORIDE 4 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (61919-565-45)
70518-1585-0 70518-1585 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20181024 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1585-0)
70518-1585-6 70518-1585 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-6)
57237-075-30 57237-075 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Rising Pharma Holdings, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (57237-075-30)
57237-075-50 57237-075 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20221004 N/A ANDA ANDA078539 Rising Pharma Holdings, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (57237-075-50)
57237-076-30 57237-076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Rising Pharma Holdings, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (57237-076-30)
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