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
51407-462-05 51407-462 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 500 TABLET, COATED in 1 BOTTLE (51407-462-05)
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)
51407-463-01 51407-463 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20210706 N/A ANDA ANDA076118 Golden State Medical Supply, Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 100 TABLET, COATED in 1 BOTTLE (51407-463-01)
50090-3243-1 50090-3243 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20171103 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE (50090-3243-1)
50090-3243-0 50090-3243 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20171117 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE (50090-3243-0)
51655-066-26 51655-066 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220711 N/A ANDA ANDA076118 Northwind Pharmaceuticals BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-066-26)
51655-065-26 51655-065 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20220527 N/A ANDA ANDA076118 Northwind Pharmaceuticals 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 Pharmaceuticals BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, COATED in 1 BOTTLE (51655-065-52)
51655-066-52 51655-066 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20160304 N/A ANDA ANDA076118 Northwind Pharmaceuticals BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE, DISPENSING (51655-066-52)
53002-1233-0 53002-1233 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20200101 N/A ANDA ANDA076118 RPK Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 100 TABLET, COATED in 1 BOTTLE (53002-1233-0)
53002-1248-0 53002-1248 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20200101 N/A ANDA ANDA076118 RPK Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 100 TABLET, COATED in 1 BOTTLE (53002-1248-0)
61919-739-90 61919-739 HUMAN PRESCRIPTION DRUG Benazepril Benazepril TABLET, COATED ORAL 20190115 N/A ANDA ANDA076118 Direct_Rx BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE (61919-739-90)
61919-756-90 61919-756 HUMAN PRESCRIPTION DRUG BENAZEPRIL HYDROCHLORIDE BENAZEPRIL HYDROCHLORIDE TABLET, COATED ORAL 20210920 N/A ANDA ANDA076118 Direct_Rx BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (61919-756-90)
63187-906-30 63187-906 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170901 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, COATED in 1 BOTTLE (63187-906-30)
63187-906-60 63187-906 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170901 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 60 TABLET, COATED in 1 BOTTLE (63187-906-60)
63187-906-90 63187-906 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170901 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (63187-906-90)
68071-1026-3 68071-1026 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170324 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 30 TABLET, COATED in 1 BOTTLE (68071-1026-3)
68071-1026-6 68071-1026 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170324 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 60 TABLET, COATED in 1 BOTTLE (68071-1026-6)
68071-1026-9 68071-1026 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170324 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (68071-1026-9)
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