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=ANDA076267"
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
62135-721-90 62135-721 HUMAN PRESCRIPTION DRUG Benazepril hydrochloride Benazepril hydrochloride TABLET ORAL 20230720 N/A ANDA ANDA076267 Chartwell RX, LLC BENAZEPRIL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (62135-721-90)
62135-722-90 62135-722 HUMAN PRESCRIPTION DRUG Benazepril hydrochloride Benazepril hydrochloride TABLET ORAL 20230720 N/A ANDA ANDA076267 Chartwell RX, LLC BENAZEPRIL HYDROCHLORIDE 40 mg/1 90 TABLET in 1 BOTTLE (62135-722-90)
62135-720-90 62135-720 HUMAN PRESCRIPTION DRUG Benazepril hydrochloride Benazepril hydrochloride TABLET ORAL 20230720 N/A ANDA ANDA076267 Chartwell RX, LLC BENAZEPRIL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (62135-720-90)
23155-750-01 23155-750 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET ORAL 20220820 N/A ANDA ANDA076267 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (23155-750-01)
23155-750-05 23155-750 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET ORAL 20220820 N/A ANDA ANDA076267 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 10 mg/1 500 TABLET in 1 BOTTLE (23155-750-05)
23155-751-01 23155-751 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET ORAL 20220820 N/A ANDA ANDA076267 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE (23155-751-01)
23155-751-05 23155-751 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET ORAL 20220820 N/A ANDA ANDA076267 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 20 mg/1 500 TABLET in 1 BOTTLE (23155-751-05)
23155-752-01 23155-752 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET ORAL 20220820 N/A ANDA ANDA076267 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 100 TABLET in 1 BOTTLE (23155-752-01)
23155-752-05 23155-752 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET ORAL 20220820 N/A ANDA ANDA076267 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 40 mg/1 500 TABLET in 1 BOTTLE (23155-752-05)
62135-719-90 62135-719 HUMAN PRESCRIPTION DRUG Benazepril hydrochloride Benazepril hydrochloride TABLET ORAL 20230720 N/A ANDA ANDA076267 Chartwell RX, LLC BENAZEPRIL HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (62135-719-90)
23155-749-05 23155-749 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET ORAL 20220820 N/A ANDA ANDA076267 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 500 TABLET in 1 BOTTLE (23155-749-05)
23155-749-01 23155-749 HUMAN PRESCRIPTION DRUG Benazepril Hydrochloride Benazepril Hydrochloride TABLET ORAL 20220820 N/A ANDA ANDA076267 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. BENAZEPRIL HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE (23155-749-01)
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