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
68071-5047-3 68071-5047 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190904 N/A ANDA ANDA078539 NuCare Pharmaceuticals,Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-5047-3)
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)
51655-016-27 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220916 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-27)
51655-016-53 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220916 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-53)
51655-016-54 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220808 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-54)
51655-016-87 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220921 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-87)
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
54348-819-02 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
50090-3185-0 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180117 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (50090-3185-0)
50090-3185-1 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-1)
50090-3185-2 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-2)
50090-3185-3 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-3)
50090-3185-4 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-4)
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)
71610-119-88 71610-119 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA078539 Aphena Pharma Solutions - Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 900 TABLET, FILM COATED in 1 BOTTLE (71610-119-88)
68071-3801-1 68071-3801 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20250224 N/A ANDA ANDA078539 NuCare Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68071-3801-1)
42708-044-05 42708-044 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180405 N/A ANDA ANDA078539 QPharma, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (42708-044-05)
16714-159-01 16714-159 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20210406 N/A ANDA ANDA078539 NorthStar Rx LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-159-01)
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)
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