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 247 条，共 13 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
71335-1357-3 71335-1357 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 8 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (71335-1357-3)
71335-1357-0 71335-1357 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 8 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (71335-1357-0)
54348-819-00 54348-819 HUMAN PRESCRIPTION DRUG Ondansetron ONDANSETRON TABLET, FILM COATED ORAL 20190710 N/A ANDA ANDA078539 PharmPak, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BOTTLE in 1 BOX (54348-819-00) / 1 TABLET, FILM COATED in 1 BOTTLE
54348-819-08 54348-819 HUMAN PRESCRIPTION DRUG Ondansetron ONDANSETRON TABLET, FILM COATED ORAL 20190710 N/A ANDA ANDA078539 PharmPak, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BOTTLE in 1 BOX (54348-819-08) / 8 TABLET, FILM COATED in 1 BOTTLE
54348-821-00 54348-821 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190808 N/A ANDA ANDA078539 Pharmpak, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 1 BOTTLE in 1 BOX (54348-821-00) / 1 TABLET, FILM COATED in 1 BOTTLE
54348-821-02 54348-821 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190808 N/A ANDA ANDA078539 Pharmpak, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 1 BOTTLE in 1 BOX (54348-821-02) / 2 TABLET, FILM COATED in 1 BOTTLE
54348-821-04 54348-821 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190808 N/A ANDA ANDA078539 Pharmpak, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 1 BOTTLE in 1 BOX (54348-821-04) / 4 TABLET, FILM COATED in 1 BOTTLE
54348-821-05 54348-821 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190808 N/A ANDA ANDA078539 Pharmpak, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 1 BOTTLE in 1 BOX (54348-821-05) / 5 TABLET, FILM COATED in 1 BOTTLE
54348-819-02 54348-819 HUMAN PRESCRIPTION DRUG Ondansetron ONDANSETRON TABLET, FILM COATED ORAL 20190710 N/A ANDA ANDA078539 PharmPak, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BOTTLE in 1 BOX (54348-819-02) / 2 TABLET, FILM COATED in 1 BOTTLE
54348-819-04 54348-819 HUMAN PRESCRIPTION DRUG Ondansetron ONDANSETRON TABLET, FILM COATED ORAL 20190710 N/A ANDA ANDA078539 PharmPak, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BOTTLE in 1 BOX (54348-819-04) / 4 TABLET, FILM COATED in 1 BOTTLE
54348-819-06 54348-819 HUMAN PRESCRIPTION DRUG Ondansetron ONDANSETRON TABLET, FILM COATED ORAL 20190710 N/A ANDA ANDA078539 PharmPak, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BOTTLE in 1 BOX (54348-819-06) / 6 TABLET, FILM COATED in 1 BOTTLE
76420-411-00 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 1000 TABLET, FILM COATED in 1 BOTTLE (76420-411-00)
76420-411-10 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 10 TABLET, FILM COATED in 1 BOTTLE (76420-411-10)
76420-411-24 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (76420-411-24)
76420-411-30 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 30 TABLET, FILM COATED in 1 BOTTLE (76420-411-30)
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)
76420-411-03 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 3 TABLET, FILM COATED in 1 BOTTLE (76420-411-03)
76420-411-05 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/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-411-05)
76420-411-06 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 6 TABLET, FILM COATED in 1 BOTTLE (76420-411-06)
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