美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CHLORPROMAZINE 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 085331 003 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 50MG No No -- Approved Prior to Jan 1, 1982 CYCLE Discontinued
CHLORPROMAZINE HYDROCHLORIDE 085331 004 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 100MG No No -- Approved Prior to Jan 1, 1982 CYCLE Discontinued
CHLORPROMAZINE HYDROCHLORIDE 085331 005 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 200MG No No -- Approved Prior to Jan 1, 1982 CYCLE Discontinued
CHLORPROMAZINE HYDROCHLORIDE 087783 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 10MG No No -- 1982/09/16 WEST WARD Discontinued
CHLORPROMAZINE HYDROCHLORIDE 087878 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 50MG No No -- 1982/09/15 WEST WARD Discontinued
CHLORPROMAZINE HYDROCHLORIDE 087880 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 200MG No No -- 1982/09/16 WEST WARD Discontinued
CHLORPROMAZINE HYDROCHLORIDE 087884 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 100MG No No -- 1982/09/15 WEST WARD Discontinued
CHLORPROMAZINE HYDROCHLORIDE 084803 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 10MG No No 1972/03/16 Approved Prior to Jan 1, 1982 LEDERLE Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080439 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1973/01/03 Approved Prior to Jan 1, 1982 SANDOZ Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080439 002 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1973/01/03 Approved Prior to Jan 1, 1982 SANDOZ Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080439 003 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1973/01/03 Approved Prior to Jan 1, 1982 SANDOZ Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080439 004 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1973/01/03 Approved Prior to Jan 1, 1982 SANDOZ Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080439 005 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1973/01/03 Approved Prior to Jan 1, 1982 SANDOZ Discontinued
CHLORPROMAZINE HYDROCHLORIDE 080365 001 ANDA CHLORPROMAZINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/ML No No 1974/02/13 Approved Prior to Jan 1, 1982 DR REDDYS Discontinued
CHLORPROMAZINE HYDROCHLORIDE 083549 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 10MG No No 1974/05/06 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
CHLORPROMAZINE HYDROCHLORIDE 083549 002 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 25MG No No 1974/05/06 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
CHLORPROMAZINE HYDROCHLORIDE 083549 003 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 50MG No No 1974/05/06 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
CHLORPROMAZINE HYDROCHLORIDE 083574 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 100MG No No 1974/05/06 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
CHLORPROMAZINE HYDROCHLORIDE 083575 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 200MG No No 1974/05/06 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
CHLORPROMAZINE HYDROCHLORIDE 083386 001 ANDA CHLORPROMAZINE HYDROCHLORIDE TABLET;ORAL 10MG Yes No 1974/07/09 Approved Prior to Jan 1, 1982 UPSHER SMITH LABS Prescription
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