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"
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
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)
60760-636-10 60760-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 St. Mary's Medical Park Pharmacy ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-10)
60760-636-16 60760-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230303 N/A ANDA ANDA078539 St. Mary's Medical Park Pharmacy ONDANSETRON HYDROCHLORIDE 4 mg/1 16 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-16)
60760-636-20 60760-636 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180326 N/A ANDA ANDA078539 St. Mary's Medical Park Pharmacy ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-20)
76420-916-05 76420-916 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-916-05)
76420-916-10 76420-916 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (76420-916-10)
76420-916-11 76420-916 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 10 BLISTER PACK in 1 CARTON (76420-916-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
76420-916-30 76420-916 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-916-30)
76420-916-33 76420-916 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 1 BLISTER PACK in 1 CARTON (76420-916-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
76420-916-60 76420-916 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-916-60)
76420-916-90 76420-916 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-916-90)
60760-658-10 60760-658 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230620 N/A ANDA ANDA078539 ST. MARY'S MEDICAL PARK PHARMACY ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-10)
60760-658-15 60760-658 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250915 N/A ANDA ANDA078539 ST. MARY'S MEDICAL PARK PHARMACY ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-15)
60760-658-20 60760-658 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA078539 ST. MARY'S MEDICAL PARK PHARMACY ONDANSETRON HYDROCHLORIDE 8 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-20)
60760-658-60 60760-658 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251030 N/A ANDA ANDA078539 ST. MARY'S MEDICAL PARK PHARMACY ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-60)
65862-187-03 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BLISTER PACK in 1 CARTON (65862-187-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK
65862-187-05 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-187-05)
65862-187-10 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 10 BLISTER PACK in 1 CARTON (65862-187-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-187-30 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-187-30)
65862-187-99 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-187-99)
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