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=ANDA210086"
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
70771-1177-0 70771-1177 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1177-0)
70771-1177-1 70771-1177 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1177-1)
70771-1178-0 70771-1178 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 150 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1178-0)
50090-6925-8 50090-6925 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20231214 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6925-8)
70771-1173-0 70771-1173 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1173-0)
60687-444-01 60687-444 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20190812 N/A ANDA ANDA210086 American Health Packaging AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-444-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-444-11)
70771-1173-1 70771-1173 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1173-1)
70771-1178-1 70771-1178 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1178-1)
60687-433-01 60687-433 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20190815 N/A ANDA ANDA210086 American Health Packaging AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-433-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-433-11)
50090-4005-0 50090-4005 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20181227 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-4005-0)
70771-1174-0 70771-1174 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1174-0)
70771-1174-1 70771-1174 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1174-1)
70771-1175-0 70771-1175 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1175-0)
70771-1175-1 70771-1175 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1175-1)
70771-1176-0 70771-1176 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 75 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1176-0)
70771-1176-1 70771-1176 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Lifesciences Limited AMITRIPTYLINE HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1176-1)
50090-4005-1 50090-4005 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-4005-1)
50090-4005-4 50090-4005 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20190212 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-4005-4)
50090-4005-8 50090-4005 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-4005-8)
16714-257-01 16714-257 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210825 N/A ANDA ANDA210086 Northstar Rx LLC. AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-257-01)
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