美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DIPHEN"
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
DIPHENHYDRAMINE HYDROCHLORIDE 080873 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 10MG/ML No No 1974/01/29 Approved Prior to Jan 1, 1982 DR REDDYS Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 080873 002 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No 1974/01/29 Approved Prior to Jan 1, 1982 DR REDDYS Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE PRESERVATIVE FREE 080873 003 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No 1974/01/29 Approved Prior to Jan 1, 1982 DR REDDYS Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 080868 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 25MG No No 1974/02/13 Approved Prior to Jan 1, 1982 LANNETT Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 080868 002 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 50MG No No 1974/02/13 Approved Prior to Jan 1, 1982 LANNETT Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 084506 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 25MG No No 1974/12/19 Approved Prior to Jan 1, 1982 MUTUAL PHARM Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 083797 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 25MG No No 1975/02/13 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 083797 002 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 50MG No No 1975/02/13 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE PRESERVATIVE FREE 084094 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No 1976/03/15 Approved Prior to Jan 1, 1982 INTL MEDICATION Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 085083 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 50MG No No 1976/06/29 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
DIPHENHYDRAMINE HYDROCHLORIDE 085138 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE;ORAL 25MG No No 1976/07/29 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
DIPHENYLAN SODIUM 080857 001 ANDA PHENYTOIN SODIUM CAPSULE;ORAL 30MG PROMPT No No 1976/12/03 Approved Prior to Jan 1, 1982 CHARTWELL MOLECULAR Discontinued
DIPHENYLAN SODIUM 080857 002 ANDA PHENYTOIN SODIUM CAPSULE;ORAL 100MG PROMPT No No 1976/12/03 Approved Prior to Jan 1, 1982 CHARTWELL MOLECULAR 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
DIPHENHYDRAMINE HYDROCHLORIDE 085621 001 ANDA DIPHENHYDRAMINE HYDROCHLORIDE ELIXIR;ORAL 12.5MG/5ML No No 1977/09/22 Approved Prior to Jan 1, 1982 KV PHARM 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
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