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=ANDA077851"
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
51407-004-05 51407-004 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET ORAL 20250107 N/A ANDA ANDA077851 Golden State Medical Supply, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 500 TABLET in 1 BOTTLE (51407-004-05)
51407-004-30 51407-004 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET ORAL 20250108 N/A ANDA ANDA077851 Golden State Medical Supply, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET in 1 BOTTLE (51407-004-30)
69339-172-03 69339-172 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET ORAL 20221024 N/A ANDA ANDA077851 Natco Pharma USA LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET in 1 BOTTLE (69339-172-03)
69339-172-05 69339-172 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET ORAL 20221024 N/A ANDA ANDA077851 Natco Pharma USA LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 500 TABLET in 1 BOTTLE (69339-172-05)
63187-236-10 63187-236 HUMAN PRESCRIPTION DRUG ONDANSETRON ONDANSETRON TABLET, FILM COATED ORAL 20140401 N/A ANDA ANDA077851 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (63187-236-10)
63187-236-15 63187-236 HUMAN PRESCRIPTION DRUG ONDANSETRON ONDANSETRON TABLET, FILM COATED ORAL 20140401 N/A ANDA ANDA077851 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (63187-236-15)
63187-236-20 63187-236 HUMAN PRESCRIPTION DRUG ONDANSETRON ONDANSETRON TABLET, FILM COATED ORAL 20140401 N/A ANDA ANDA077851 Proficient Rx LP ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (63187-236-20)
45963-539-30 45963-539 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20070727 N/A ANDA ANDA077851 ACTAVIS PHARMA, INC. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (45963-539-30)
51407-003-05 51407-003 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET ORAL 20250107 N/A ANDA ANDA077851 Golden State Medical Supply, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET in 1 BOTTLE (51407-003-05)
51407-003-30 51407-003 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET ORAL 20250108 N/A ANDA ANDA077851 Golden State Medical Supply, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET in 1 BOTTLE (51407-003-30)
69339-171-03 69339-171 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET ORAL 20221024 N/A ANDA ANDA077851 Natco Pharma USA LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET in 1 BOTTLE (69339-171-03)
69339-171-05 69339-171 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET ORAL 20221024 N/A ANDA ANDA077851 Natco Pharma USA LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET in 1 BOTTLE (69339-171-05)
63850-0003-1 63850-0003 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron Tablets TABLET, FILM COATED ORAL 20070625 N/A ANDA ANDA077851 Natco Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63850-0003-1)
71335-0815-0 71335-0815 HUMAN PRESCRIPTION DRUG ondansetron ondansetron hydrochloride TABLET, FILM COATED ORAL 20120824 N/A ANDA ANDA077851 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 8 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (71335-0815-0)
71335-0815-1 71335-0815 HUMAN PRESCRIPTION DRUG ondansetron ondansetron hydrochloride TABLET, FILM COATED ORAL 20120824 N/A ANDA ANDA077851 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-0815-1)
71335-0815-2 71335-0815 HUMAN PRESCRIPTION DRUG ondansetron ondansetron hydrochloride TABLET, FILM COATED ORAL 20120824 N/A ANDA ANDA077851 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-0815-2)
71335-0815-3 71335-0815 HUMAN PRESCRIPTION DRUG ondansetron ondansetron hydrochloride TABLET, FILM COATED ORAL 20120824 N/A ANDA ANDA077851 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 8 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (71335-0815-3)
45963-538-30 45963-538 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20070727 N/A ANDA ANDA077851 ACTAVIS PHARMA, INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (45963-538-30)
63850-0004-1 63850-0004 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron Tablets TABLET, FILM COATED ORAL 20070625 N/A ANDA ANDA077851 Natco Pharma Limited ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63850-0004-1)
63304-459-30 63304-459 HUMAN PRESCRIPTION DRUG ONDANSETRON ONDANSETRON TABLET, FILM COATED ORAL 20070625 N/A ANDA ANDA077851 Sun Pharmaceutical Industries, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63304-459-30)
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