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"
符合检索条件的记录共 49 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
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)
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)
70710-1227-0 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)
70710-1227-1 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/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1227-1)
70710-1228-0 70710-1228 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 75 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1228-0)
70710-1228-1 70710-1228 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1228-1)
70710-1229-0 70710-1229 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1229-0)
70710-1229-1 70710-1229 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1229-1)
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)
70710-1230-1 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/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1230-1)
68071-3913-3 68071-3913 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20251110 N/A ANDA ANDA210086 NuCare Pharmaceuticals, Inc. AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3913-3)
70710-1225-1 70710-1225 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1225-1)
70710-1225-0 70710-1225 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20171226 N/A ANDA ANDA210086 Zydus Pharmaceuticals USA Inc. AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1225-0)
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)
16714-259-01 16714-259 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210825 N/A ANDA ANDA210086 Northstar Rx LLC. AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-259-01)
16714-259-02 16714-259 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210825 N/A ANDA ANDA210086 Northstar Rx LLC. AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16714-259-02)
16714-260-01 16714-260 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210825 N/A ANDA ANDA210086 Northstar Rx LLC. AMITRIPTYLINE HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-260-01)
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)
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)
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