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=ANDA090168"
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
63187-840-03 63187-840 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20170501 N/A ANDA ANDA090168 Proficient Rx LP BENZTROPINE MESYLATE 1 mg/1 3 TABLET in 1 BOTTLE (63187-840-03)
63187-840-30 63187-840 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20170501 N/A ANDA ANDA090168 Proficient Rx LP BENZTROPINE MESYLATE 1 mg/1 30 TABLET in 1 BOTTLE (63187-840-30)
63187-840-60 63187-840 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20170501 N/A ANDA ANDA090168 Proficient Rx LP BENZTROPINE MESYLATE 1 mg/1 90 TABLET in 1 BOTTLE (63187-840-60)
63187-840-90 63187-840 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20170501 N/A ANDA ANDA090168 Proficient Rx LP BENZTROPINE MESYLATE 1 mg/1 60 TABLET in 1 BOTTLE (63187-840-90)
70518-0577-0 70518-0577 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20170619 N/A ANDA ANDA090168 REMEDYREPACK INC. BENZTROPINE MESYLATE 1 mg/1 30 TABLET in 1 BLISTER PACK (70518-0577-0)
70518-0577-2 70518-0577 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20200609 N/A ANDA ANDA090168 REMEDYREPACK INC. BENZTROPINE MESYLATE 1 mg/1 30 TABLET in 1 BLISTER PACK (70518-0577-2)
70518-0577-3 70518-0577 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20220203 N/A ANDA ANDA090168 REMEDYREPACK INC. BENZTROPINE MESYLATE 1 mg/1 100 POUCH in 1 BOX (70518-0577-3) / 1 TABLET in 1 POUCH (70518-0577-4)
69315-136-01 69315-136 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20160515 N/A ANDA ANDA090168 Leading Pharma, LLC BENZTROPINE MESYLATE .5 mg/1 100 TABLET in 1 BOTTLE (69315-136-01)
69315-136-10 69315-136 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20160515 N/A ANDA ANDA090168 Leading Pharma, LLC BENZTROPINE MESYLATE .5 mg/1 1000 TABLET in 1 BOTTLE (69315-136-10)
69315-137-01 69315-137 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20160515 N/A ANDA ANDA090168 Leading Pharma, LLC BENZTROPINE MESYLATE 1 mg/1 100 TABLET in 1 BOTTLE (69315-137-01)
69315-137-10 69315-137 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20160515 N/A ANDA ANDA090168 Leading Pharma, LLC BENZTROPINE MESYLATE 1 mg/1 1000 TABLET in 1 BOTTLE (69315-137-10)
69315-138-01 69315-138 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20160515 N/A ANDA ANDA090168 Leading Pharma, LLC BENZTROPINE MESYLATE 2 mg/1 100 TABLET in 1 BOTTLE (69315-138-01)
69315-138-10 69315-138 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20160515 N/A ANDA ANDA090168 Leading Pharma, LLC BENZTROPINE MESYLATE 2 mg/1 1000 TABLET in 1 BOTTLE (69315-138-10)
71610-502-53 71610-502 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20201208 N/A ANDA ANDA090168 Aphena Pharma Solutions - Tennessee, LLC BENZTROPINE MESYLATE 1 mg/1 60 TABLET in 1 BOTTLE (71610-502-53)
70518-2677-0 70518-2677 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20200408 N/A ANDA ANDA090168 REMEDYREPACK INC. BENZTROPINE MESYLATE 2 mg/1 30 TABLET in 1 BLISTER PACK (70518-2677-0)
70518-2677-1 70518-2677 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20201005 N/A ANDA ANDA090168 REMEDYREPACK INC. BENZTROPINE MESYLATE 2 mg/1 30 TABLET in 1 BLISTER PACK (70518-2677-1)
70518-2732-0 70518-2732 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20200511 N/A ANDA ANDA090168 REMEDYREPACK INC. BENZTROPINE MESYLATE .5 mg/1 30 TABLET in 1 BLISTER PACK (70518-2732-0)
70518-2732-2 70518-2732 HUMAN PRESCRIPTION DRUG BENZTROPINE MESYLATE BENZTROPINE MESYLATE TABLET ORAL 20201218 N/A ANDA ANDA090168 REMEDYREPACK INC. BENZTROPINE MESYLATE .5 mg/1 60 TABLET in 1 BLISTER PACK (70518-2732-2)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase