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 255 条，共 13 页，当前第 11 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
76420-411-60 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-411-60)
76420-411-90 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-411-90)
71335-1855-6 71335-1855 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20211221 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (71335-1855-6)
71335-1855-7 71335-1855 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20211221 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1855-7)
71335-1855-8 71335-1855 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20211221 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (71335-1855-8)
71335-1855-9 71335-1855 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20211221 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1855-9)
43063-792-06 43063-792 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171006 N/A ANDA ANDA078539 PD-Rx Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-792-06)
85509-1076-1 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (85509-1076-1)
85509-1076-2 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (85509-1076-2)
85509-1076-3 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85509-1076-3)
85509-1076-5 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (85509-1076-5)
85509-1076-6 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (85509-1076-6)
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)
50268-622-15 50268-622 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20160805 N/A ANDA ANDA078539 AvPAK ONDANSETRON HYDROCHLORIDE 8 mg/1 50 BLISTER PACK in 1 BOX (50268-622-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-622-11)
51655-415-04 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180412 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (51655-415-04)
51655-415-43 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171228 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (51655-415-43)
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