美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=PROMAZINE HYDROCHLORIDE"
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
CHLORPROMAZINE HYDROCHLORIDE 080340 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 PVT FORM Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080340 002 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 50MG No No -- Approved Prior to Jan 1, 1982 PVT FORM Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080340 003 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 200MG No No -- Approved Prior to Jan 1, 1982 PVT FORM Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080370 001 ANDA CHLORPROMAZINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/ML No No -- Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080403 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 PUREPAC PHARM Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080403 002 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 50MG No No -- Approved Prior to Jan 1, 1982 PUREPAC PHARM Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080403 003 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 100MG No No -- Approved Prior to Jan 1, 1982 PUREPAC PHARM Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080403 004 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 10MG No No -- Approved Prior to Jan 1, 1982 PUREPAC PHARM Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080403 005 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 200MG No No -- Approved Prior to Jan 1, 1982 PUREPAC PHARM Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084411 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 50MG No No -- Approved Prior to Jan 1, 1982 ABBOTT Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084412 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 100MG No No -- Approved Prior to Jan 1, 1982 ABBOTT Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084413 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 200MG No No -- Approved Prior to Jan 1, 1982 ABBOTT Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084414 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 10MG No No -- Approved Prior to Jan 1, 1982 ABBOTT Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084415 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 ABBOTT Discontinued
PROMAZINE HYDROCHLORIDE 084510 001 ANDA PROMAZINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/ML No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
PROMAZINE HYDROCHLORIDE 084517 001 ANDA PROMAZINE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML No No -- Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084789 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 100MG No No -- Approved Prior to Jan 1, 1982 LEDERLE Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084800 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 50MG No No -- Approved Prior to Jan 1, 1982 LEDERLE Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084801 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 LEDERLE Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084802 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 200MG No No -- Approved Prior to Jan 1, 1982 LEDERLE Discontinued
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