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=ANDA076118"
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
71335-0078-1 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE (71335-0078-1)
71335-0078-2 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 60 TABLET, COATED in 1 BOTTLE (71335-0078-2)
71335-0078-3 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 100 TABLET, COATED in 1 BOTTLE (71335-0078-3)
71335-0078-4 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE (71335-0078-4)
71335-0078-5 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 14 TABLET, COATED in 1 BOTTLE (71335-0078-5)
71335-0078-6 71335-0078 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220209 N/A ANDA ANDA076118 Bryant Ranch Prepack BENAZEPRIL HYDROCHLORIDE 20 mg/1 10 TABLET, COATED in 1 BOTTLE (71335-0078-6)
51655-065-26 51655-065 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220527 N/A ANDA ANDA076118 Northwind Health Company, LLC BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-065-26)
51655-065-52 51655-065 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20160623 N/A ANDA ANDA076118 Northwind Health Company, LLC BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, COATED in 1 BOTTLE (51655-065-52)
51407-465-01 51407-465 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET, COATED in 1 BOTTLE (51407-465-01)
51407-465-05 51407-465 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 500 TABLET, COATED in 1 BOTTLE (51407-465-05)
51655-066-26 51655-066 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220711 N/A ANDA ANDA076118 Northwind Health Company, LLC BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-066-26)
51655-066-52 51655-066 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20160304 N/A ANDA ANDA076118 Northwind Health Company, LLC BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE, DISPENSING (51655-066-52)
68788-6889-1 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 100 TABLET, COATED in 1 BOTTLE (68788-6889-1)
68788-6889-3 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 30 TABLET, COATED in 1 BOTTLE (68788-6889-3)
68788-6889-6 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 60 TABLET, COATED in 1 BOTTLE (68788-6889-6)
68788-6889-8 68788-6889 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170206 N/A ANDA ANDA076118 Preferred Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 120 TABLET, COATED in 1 BOTTLE (68788-6889-8)
68788-9327-1 68788-9327 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20150325 N/A ANDA ANDA076118 Preferred Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 100 TABLET, COATED in 1 BOTTLE (68788-9327-1)
68788-9327-3 68788-9327 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20150325 N/A ANDA ANDA076118 Preferred Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, COATED in 1 BOTTLE (68788-9327-3)
68788-9327-6 68788-9327 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20150325 N/A ANDA ANDA076118 Preferred Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 60 TABLET, COATED in 1 BOTTLE (68788-9327-6)
68788-9327-9 68788-9327 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20150325 N/A ANDA ANDA076118 Preferred Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, COATED in 1 BOTTLE (68788-9327-9)
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