美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=ATROPINE"
符合检索条件的记录共 77 条
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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
MEPERIDINE AND ATROPINE SULFATE 085121 001 ANDA ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE INJECTABLE;INJECTION 0.4MG/ML;50MG/ML No No -- Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
MEPERIDINE AND ATROPINE SULFATE 085121 002 ANDA ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE INJECTABLE;INJECTION 0.4MG/ML;75MG/ML No No -- Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
MEPERIDINE AND ATROPINE SULFATE 085121 003 ANDA ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE INJECTABLE;INJECTION 0.4MG/ML;100MG/ML No No -- Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
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
ATROPINE AND DEMEROL 087847 001 ANDA ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE INJECTABLE;INJECTION 0.4MG/ML;75MG/ML No No -- 1982/11/26 ABBVIE Discontinued
ATROPINE AND DEMEROL 087848 001 ANDA ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE INJECTABLE;INJECTION 0.4MG/ML;100MG/ML No No -- 1982/11/26 ABBVIE Discontinued
ATROPINE AND DEMEROL 087853 001 ANDA ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE INJECTABLE;INJECTION 0.4MG/ML;50MG/ML No No -- 1982/11/26 ABBVIE 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 Discontinued
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 Discontinued
DIPHENOXYLATE HYDROCHLORIDE W/ ATROPINE SULFATE 086440 001 ANDA ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE CAPSULE;ORAL 0.025MG;2.5MG No No 1981/04/06 Approved Prior to Jan 1, 1982 SCHERER RP Discontinued
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