美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 040395 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2000/11/27 2000/11/27 ABLE Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 210571 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2018/08/31 2018/08/31 UPSHER SMITH LABS Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 210819 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2018/11/13 2018/11/13 BAYSHORE PHARMS LLC Prescription
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 213413 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2020/02/20 2020/02/20 LEADING Prescription
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 210789 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2020/06/03 2020/06/03 DR REDDYS LABS SA Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 213335 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2020/10/06 2020/10/06 SPECGX LLC Prescription
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 207128 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2020/10/21 2020/10/21 CHARTWELL RX Prescription
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 211362 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2021/01/27 2021/01/27 WINDER LABS LLC Prescription
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