美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=CARDIZEM"
符合检索条件的记录共 22 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
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HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/01/23 1989/01/23 BIOVAIL Discontinued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HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/01/23 1989/01/23 BIOVAIL Discontinued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CAPSULE, EXTENDED RELEASE;ORAL 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/01/23 1989/01/23 BIOVAIL Discontinued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CAPSULE, EXTENDED RELEASE;ORAL 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/01/23 1989/01/23 BIOVAIL Discontinued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HYDROCHLORIDE INJECTABLE;INJECTION 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1991/10/24 1991/10/24 BIOVAIL LABS INTL Discontinued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HYDROCHLORIDE INJECTABLE;INJECTION 25MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1991/10/24 1995/08/18 BIOVAIL LABS INTL Discontinued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
CARDIZEM 020792 001 NDA DILTIAZEM HYDROCHLORIDE INJECTABLE;INJECTION 100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1997/09/05 1997/09/05 BIOVAIL Discontinued
CARDIZEM LA 021392 001 NDA DILTIAZEM HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 120MG Yes No 2003/02/06 2003/02/06 BAUSCH Prescription
CARDIZEM LA 021392 002 NDA DILTIAZEM HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 180MG Yes No 2003/02/06 2003/02/06 BAUSCH Prescription
CARDIZEM LA 021392 003 NDA DILTIAZEM HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 240MG Yes No 2003/02/06 2003/02/06 BAUSCH Prescription
CARDIZEM LA 021392 004 NDA DILTIAZEM HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 300MG Yes No 2003/02/06 2003/02/06 BAUSCH Prescription
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