美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:药品名称,活性成分,申请号中含有 "diltiazem"
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
DILTIAZEM HYDROCHLORIDE 074084 001 ANDA DILTIAZEM HYDROCHLORIDE TABLET;ORAL 30MG No No -- 1994/02/25 TEVA Discontinued
DILTIAZEM HYDROCHLORIDE 074084 002 ANDA DILTIAZEM HYDROCHLORIDE TABLET;ORAL 60MG No No -- 1994/02/25 TEVA Discontinued
CARDIZEM 018602 001 NDA DILTIAZEM HYDROCHLORIDE TABLET;ORAL 30MG Yes No 1982/11/05 1982/11/05 BAUSCH Prescription
CARDIZEM 018602 002 NDA DILTIAZEM HYDROCHLORIDE TABLET;ORAL 60MG Yes No 1982/11/05 1982/11/05 BAUSCH Prescription
CARDIZEM 018602 003 NDA DILTIAZEM HYDROCHLORIDE TABLET;ORAL 90MG Yes No 1982/11/05 1986/12/08 BAUSCH Prescription
CARDIZEM 018602 004 NDA DILTIAZEM HYDROCHLORIDE TABLET;ORAL 120MG Yes Yes 1982/11/05 1986/12/08 BAUSCH Prescription
CARDIZEM SR 019471 001 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/01/23 1989/01/23 BIOVAIL Discontinued
CARDIZEM SR 019471 002 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/01/23 1989/01/23 BIOVAIL Discontinued
CARDIZEM SR 019471 003 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/01/23 1989/01/23 BIOVAIL Discontinued
CARDIZEM SR 019471 004 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/01/23 1989/01/23 BIOVAIL Discontinued
CARDIZEM 020027 001 NDA DILTIAZEM HYDROCHLORIDE INJECTABLE;INJECTION 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1991/10/24 1991/10/24 BIOVAIL LABS INTL Discontinued
CARDIZEM 020027 003 NDA DILTIAZEM HYDROCHLORIDE INJECTABLE;INJECTION 25MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1991/10/24 1995/08/18 BIOVAIL LABS INTL Discontinued
CARDIZEM CD 020062 001 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 120MG Yes No 1991/12/27 1992/08/10 BAUSCH Prescription
CARDIZEM CD 020062 002 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 180MG Yes No 1991/12/27 1991/12/27 BAUSCH Prescription
CARDIZEM CD 020062 003 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 240MG Yes No 1991/12/27 1991/12/27 BAUSCH Prescription
CARDIZEM CD 020062 004 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 300MG Yes No 1991/12/27 1991/12/27 BAUSCH Prescription
CARDIZEM CD 020062 005 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 360MG Yes Yes 1991/12/27 1999/08/24 BAUSCH Prescription
DILACOR XR 020092 001 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1992/05/29 1992/05/29 ALLERGAN Discontinued
DILACOR XR 020092 002 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1992/05/29 1992/05/29 ALLERGAN Discontinued
DILACOR XR 020092 003 NDA DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1992/05/29 1992/05/29 ALLERGAN Discontinued
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