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=ANDA077584"
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
63187-190-30 63187-190 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-190-30)
63187-190-60 63187-190 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-190-60)
63187-190-90 63187-190 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-190-90)
60760-501-90 60760-501 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20190320 N/A ANDA ANDA077584 St. Mary's Medical Park Pharmacy PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-501-90)
68788-7410-1 68788-7410 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180606 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7410-1)
68788-7410-2 68788-7410 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180606 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 30 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68788-7410-2)
68788-7410-3 68788-7410 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180606 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7410-3)
68788-7410-6 68788-7410 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180606 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 30 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7410-6)
68788-7410-8 68788-7410 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180606 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 30 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-7410-8)
68788-7410-9 68788-7410 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20180606 N/A ANDA ANDA077584 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7410-9)
72189-492-30 72189-492 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20230621 N/A ANDA ANDA077584 Direct_Rx PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-492-30)
63187-434-30 63187-434 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-434-30)
63187-434-60 63187-434 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-434-60)
63187-434-90 63187-434 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20150202 N/A ANDA ANDA077584 Proficient Rx LP PAROXETINE HYDROCHLORIDE HEMIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-434-90)
70518-3430-1 70518-3430 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220624 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3430-1)
70518-3430-2 70518-3430 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20250801 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3430-2)
70518-3518-0 70518-3518 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220913 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-0)
70518-3518-1 70518-3518 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20220929 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3518-1)
70518-3518-2 70518-3518 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20250131 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 100 POUCH in 1 BOX (70518-3518-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-3518-3)
70518-3518-4 70518-3518 HUMAN PRESCRIPTION DRUG Paroxetine Paroxetine TABLET, FILM COATED ORAL 20250618 N/A ANDA ANDA077584 REMEDYREPACK INC. PAROXETINE HYDROCHLORIDE HEMIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-4)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase