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 086057 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No -- Approved Prior to Jan 1, 1982 ROXANE Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 086798 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No -- Approved Prior to Jan 1, 1982 HEATHER Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 086950 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No -- Approved Prior to Jan 1, 1982 LEDERLE Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 087934 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No -- 1983/07/19 ASCOT Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 085506 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1977/06/03 Approved Prior to Jan 1, 1982 SUN PHARM INDUSTRIES Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 085035 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1977/07/05 Approved Prior to Jan 1, 1982 R AND S PHARMA Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 085762 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1977/11/17 Approved Prior to Jan 1, 1982 MYLAN Prescription
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 085659 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1978/01/27 Approved Prior to Jan 1, 1982 KV PHARM Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 085372 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1978/02/21 Approved Prior to Jan 1, 1982 LANNETT Prescription
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 085509 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1978/03/09 Approved Prior to Jan 1, 1982 INWOOD LABS Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 085876 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1978/06/22 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 085766 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1978/12/22 Approved Prior to Jan 1, 1982 PVT FORM Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 086727 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1979/10/29 Approved Prior to Jan 1, 1982 ANI PHARMS INC Prescription
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 087131 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1981/07/17 Approved Prior to Jan 1, 1982 PARKE DAVIS Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 086173 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1981/08/28 Approved Prior to Jan 1, 1982 FOSUN PHARMA Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 087765 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1982/03/15 1982/03/15 HIKMA PHARMS Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 087842 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1982/03/29 1982/03/29 USL PHARMA Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 087708 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE SOLUTION;ORAL 0.025MG/5ML;2.5MG/5ML No Yes 1982/05/03 1982/05/03 HIKMA Prescription
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 087195 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 1997/03/05 1982/02/16 VALEANT PHARM INTL Discontinued
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 040357 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE TABLET;ORAL 0.025MG;2.5MG No No 2000/05/02 2000/05/02 PAR PHARM Prescription
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