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=ANDA074787"
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
23155-723-01 23155-723 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20200222 N/A ANDA ANDA074787 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. LABETALOL HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (23155-723-01)
23155-723-05 23155-723 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20200222 N/A ANDA ANDA074787 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. LABETALOL HYDROCHLORIDE 100 mg/1 500 TABLET in 1 BOTTLE (23155-723-05)
23155-724-01 23155-724 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20200222 N/A ANDA ANDA074787 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. LABETALOL HYDROCHLORIDE 200 mg/1 100 TABLET in 1 BOTTLE (23155-724-01)
23155-724-05 23155-724 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20200222 N/A ANDA ANDA074787 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. LABETALOL HYDROCHLORIDE 200 mg/1 500 TABLET in 1 BOTTLE (23155-724-05)
23155-725-01 23155-725 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20200222 N/A ANDA ANDA074787 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. LABETALOL HYDROCHLORIDE 300 mg/1 100 TABLET in 1 BOTTLE (23155-725-01)
23155-725-05 23155-725 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20200222 N/A ANDA ANDA074787 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. LABETALOL HYDROCHLORIDE 300 mg/1 500 TABLET in 1 BOTTLE (23155-725-05)
62135-791-60 62135-791 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20231024 N/A ANDA ANDA074787 Chartwell RX, LLC LABETALOL HYDROCHLORIDE 100 mg/1 60 TABLET in 1 BOTTLE (62135-791-60)
62135-792-60 62135-792 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20231024 N/A ANDA ANDA074787 Chartwell RX, LLC LABETALOL HYDROCHLORIDE 200 mg/1 60 TABLET in 1 BOTTLE (62135-792-60)
62135-800-60 62135-800 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET ORAL 20231024 N/A ANDA ANDA074787 Chartwell RX, LLC LABETALOL HYDROCHLORIDE 300 mg/1 60 TABLET in 1 BOTTLE (62135-800-60)
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