美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=MINOCIN"
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
MINOCIN 062139 001 ANDA MINOCYCLINE HYDROCHLORIDE INJECTABLE;INJECTION EQ 100MG BASE/VIAL No No -- Approved Prior to Jan 1, 1982 LEDERLE Discontinued
MINOCIN 050315 001 NDA MINOCYCLINE HYDROCHLORIDE CAPSULE;ORAL EQ 100MG BASE No No 1971/06/30 Approved Prior to Jan 1, 1982 TRIAX PHARMS Discontinued
MINOCIN 050315 002 NDA MINOCYCLINE HYDROCHLORIDE CAPSULE;ORAL EQ 50MG BASE No No 1971/06/30 Approved Prior to Jan 1, 1982 TRIAX PHARMS Discontinued
MINOCIN 050444 001 NDA MINOCYCLINE HYDROCHLORIDE INJECTABLE;INJECTION EQ 100MG BASE/VIAL Yes Yes 1972/10/26 Approved Prior to Jan 1, 1982 REMPEX Prescription
MINOCIN 050445 001 NDA MINOCYCLINE HYDROCHLORIDE SUSPENSION;ORAL EQ 50MG BASE/5ML No No 1972/10/26 Approved Prior to Jan 1, 1982 BAUSCH Discontinued
MINOCIN 050649 001 NDA MINOCYCLINE HYDROCHLORIDE CAPSULE;ORAL EQ 50MG BASE Yes No 1990/05/31 1990/05/31 BAUSCH Prescription
MINOCIN 050649 002 NDA MINOCYCLINE HYDROCHLORIDE CAPSULE;ORAL EQ 100MG BASE Yes No 1990/05/31 1990/05/31 BAUSCH Prescription
MINOCIN 050649 003 NDA MINOCYCLINE HYDROCHLORIDE CAPSULE;ORAL EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1990/05/31 2001/02/12 BAUSCH Discontinued
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