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=ANDA075133"
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
0591-0605-01 0591-0605 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-01)
0591-0605-05 0591-0605 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-05)
0591-0605-10 0591-0605 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-10)
0591-0606-01 0591-0606 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0606-01)
0591-0606-05 0591-0606 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0606-05)
0591-0606-10 0591-0606 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0606-10)
0591-0607-01 0591-0607 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0607-01)
0591-0607-05 0591-0607 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0607-05)
0591-0607-10 0591-0607 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 19980803 N/A ANDA ANDA075133 Actavis Pharma, Inc. LABETALOL HYDROCHLORIDE 300 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0607-10)
50090-6777-0 50090-6777 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20231025 N/A ANDA ANDA075133 A-S Medication Solutions LABETALOL HYDROCHLORIDE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-6777-0)
50090-6777-1 50090-6777 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20231025 N/A ANDA ANDA075133 A-S Medication Solutions LABETALOL HYDROCHLORIDE 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6777-1)
50090-6778-0 50090-6778 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20231025 N/A ANDA ANDA075133 A-S Medication Solutions LABETALOL HYDROCHLORIDE 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6778-0)
50090-6785-0 50090-6785 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20231030 N/A ANDA ANDA075133 A-S Medication Solutions LABETALOL HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6785-0)
50090-7156-0 50090-7156 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20240430 N/A ANDA ANDA075133 A-S Medication Solutions LABETALOL HYDROCHLORIDE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-0)
50090-7156-1 50090-7156 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20240430 N/A ANDA ANDA075133 A-S Medication Solutions LABETALOL HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-1)
71205-095-30 71205-095 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA075133 Proficient Rx LP LABETALOL HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-30)
71205-095-60 71205-095 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA075133 Proficient Rx LP LABETALOL HYDROCHLORIDE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-60)
71205-095-90 71205-095 HUMAN PRESCRIPTION DRUG Labetalol hydrochloride Labetalol hydrochloride TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA075133 Proficient Rx LP LABETALOL HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-90)
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