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
70771-1174-0 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)
70771-1178-0 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)
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)
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)
16714-257-02 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 1000 TABLET, FILM COATED in 1 BOTTLE (16714-257-02)
16714-261-01 16714-261 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210825 N/A ANDA ANDA210086 Northstar Rx LLC. AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-261-01)
70710-1226-0 70710-1226 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1226-0)
70710-1226-1 70710-1226 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1226-1)
70710-1230-0 70710-1230 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 150 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1230-0)
50090-7183-0 50090-7183 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20240618 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-7183-0)
50090-7183-1 50090-7183 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20240618 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7183-1)
50090-7183-2 50090-7183 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20240618 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-7183-2)
50090-7183-5 50090-7183 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20240618 N/A ANDA ANDA210086 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7183-5)
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)
16714-258-01 16714-258 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210825 N/A ANDA ANDA210086 Northstar Rx LLC. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-258-01)
16714-258-02 16714-258 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210825 N/A ANDA ANDA210086 Northstar Rx LLC. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16714-258-02)
16714-262-01 16714-262 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210825 N/A ANDA ANDA210086 Northstar Rx LLC. AMITRIPTYLINE HYDROCHLORIDE 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-262-01)
70710-1227-0 70710-1227 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1227-0)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase