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=ANDA078406"
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
70518-2574-3 70518-2574 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20240122 N/A ANDA ANDA078406 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2574-3)
70518-2574-1 70518-2574 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20200902 N/A ANDA ANDA078406 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 POUCH in 1 BOX (70518-2574-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2574-2)
13107-154-30 13107-154 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13107-154-30)
13107-154-90 13107-154 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13107-154-90)
13107-154-99 13107-154 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13107-154-99)
13107-155-01 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13107-155-01)
13107-155-05 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13107-155-05)
13107-155-30 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13107-155-30)
13107-155-90 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13107-155-90)
13107-155-99 13107-155 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13107-155-99)
13107-156-01 13107-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13107-156-01)
13107-156-05 13107-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13107-156-05)
13107-156-30 13107-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13107-156-30)
13107-156-90 13107-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13107-156-90)
13107-156-99 13107-156 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13107-156-99)
13107-157-01 13107-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13107-157-01)
13107-157-05 13107-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13107-157-05)
13107-157-30 13107-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13107-157-30)
13107-157-90 13107-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13107-157-90)
13107-157-99 13107-157 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20091203 N/A ANDA ANDA078406 Aurolife Pharma LLC PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13107-157-99)
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