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 262 条，共 14 页，当前第 2 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
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)
16714-160-01 16714-160 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20210406 N/A ANDA ANDA078539 NorthStar Rx LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-160-01)
63187-636-01 63187-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180904 N/A ANDA ANDA078539 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 1 TABLET, FILM COATED in 1 BOTTLE (63187-636-01)
63187-636-03 63187-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20170501 N/A ANDA ANDA078539 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (63187-636-03)
63187-636-06 63187-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190801 N/A ANDA ANDA078539 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (63187-636-06)
63187-636-10 63187-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20160502 N/A ANDA ANDA078539 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 10 BLISTER PACK in 1 CARTON (63187-636-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70518-3511-0 70518-3511 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220906 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-0)
70518-3511-1 70518-3511 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250702 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-1)
50268-621-15 50268-621 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20160805 N/A ANDA ANDA078539 AvPAK ONDANSETRON HYDROCHLORIDE 4 mg/1 50 BLISTER PACK in 1 BOX (50268-621-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-621-11)
68788-9402-1 68788-9402 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20120612 N/A ANDA ANDA078539 Preferred Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68788-9402-1)
68788-9402-2 68788-9402 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20170623 N/A ANDA ANDA078539 Preferred Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68788-9402-2)
68788-9402-3 68788-9402 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20120612 N/A ANDA ANDA078539 Preferred Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-9402-3)
68788-9402-5 68788-9402 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20170623 N/A ANDA ANDA078539 Preferred Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-9402-5)
68788-9402-6 68788-9402 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20170623 N/A ANDA ANDA078539 Preferred Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68788-9402-6)
71335-0205-0 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180405 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0205-0)
63187-636-12 63187-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180904 N/A ANDA ANDA078539 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (63187-636-12)
63187-636-15 63187-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20160502 N/A ANDA ANDA078539 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (63187-636-15)
70518-1585-2 70518-1585 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20210203 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-2)
70518-1585-3 70518-1585 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-3)
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