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"
符合检索条件的记录共 95 条，共 5 页，当前第 3 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
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)
68788-6889-9 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 90 TABLET, COATED in 1 BOTTLE (68788-6889-9)
51407-462-01 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/1 100 TABLET, COATED in 1 BOTTLE (51407-462-01)
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)
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)
50090-0914-1 50090-0914 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20141128 N/A ANDA ANDA076118 A-S Medication Solutions BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (50090-0914-1)
43063-677-30 43063-677 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20160609 N/A ANDA ANDA076118 PD-Rx Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-677-30)
43063-677-90 43063-677 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20240607 N/A ANDA ANDA076118 PD-Rx Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-677-90)
68071-5130-0 68071-5130 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20191212 N/A ANDA ANDA076118 NuCare Pharmaceuticals,Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 100 TABLET, COATED in 1 BOTTLE (68071-5130-0)
63187-499-30 63187-499 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20150202 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 10 mg/1 30 TABLET, COATED in 1 BOTTLE (63187-499-30)
63187-499-60 63187-499 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20150202 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 10 mg/1 60 TABLET, COATED in 1 BOTTLE (63187-499-60)
63187-499-90 63187-499 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20150202 N/A ANDA ANDA076118 Proficient Rx LP BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET, COATED in 1 BOTTLE (63187-499-90)
68071-1769-1 68071-1769 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20191018 N/A ANDA ANDA076118 NuCare Pharmaceuticals,Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 100 TABLET, COATED in 1 BOTTLE (68071-1769-1)
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)
68071-3324-1 68071-3324 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170710 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 120 TABLET, COATED in 1 BOTTLE (68071-3324-1)
68071-3324-3 68071-3324 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170710 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 30 TABLET, COATED in 1 BOTTLE (68071-3324-3)
68071-3324-6 68071-3324 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET, COATED ORAL 20170710 N/A ANDA ANDA076118 NuCare Pharmaceuticals, Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 60 TABLET, COATED in 1 BOTTLE (68071-3324-6)
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