Drug class

Immunosuppressive Inosine Monophosphate Dehydrogenase Inhib.

The class "Immunosuppressive Inosine Monophosphate Dehydrogenase Inhib." (or immunosuppressive inosine monophosphate dehydrogenase inhibitors) is a standard formulary classification for antiproliferative immunosuppressant agents, principally represented by mycophenolate mofetil and mycophenolic acid. Read more about Immunosuppressive Inosine Monophosphate Dehydrogenase Inhib.

56 drugs in this class 40 manufacturers

Advertisement

Drugs in Immunosuppressive Inosine Monophosphate Dehydrogenase Inhib.

Showing 28–36 of 56 drugs

MYCOPHENOLATE MOFETIL

IMMUNOSUPPRESSIVE INOSINE MONOPHOSPHATE DEHYDROGENASE INHIB. · PREVENTION OF KIDNEY TRANSPLANT REJECTION ·+2
Lannett Company

MYCOPHENOLATE MOFETIL

IMMUNOSUPPRESSIVE INOSINE MONOPHOSPHATE DEHYDROGENASE INHIB. · PREVENTION OF KIDNEY TRANSPLANT REJECTION ·+2
Major Pharamceuticals

MYCOPHENOLATE MOFETIL

IMMUNOSUPPRESSIVE INOSINE MONOPHOSPHATE DEHYDROGENASE INHIB. · PREVENTION OF KIDNEY TRANSPLANT REJECTION ·+2
CAMBER PHARMACE

MYCOPHENOLATE MOFETIL

IMMUNOSUPPRESSIVE INOSINE MONOPHOSPHATE DEHYDROGENASE INHIB. · PREVENTION OF KIDNEY TRANSPLANT REJECTION ·+2
AVPAK

MYCOPHENOLATE MOFETIL

IMMUNOSUPPRESSIVE INOSINE MONOPHOSPHATE DEHYDROGENASE INHIB. · PREVENTION OF KIDNEY TRANSPLANT REJECTION ·+2
PROFICIENT RX L

MYCOPHENOLATE MOFETIL

IMMUNOSUPPRESSIVE INOSINE MONOPHOSPHATE DEHYDROGENASE INHIB. · PREVENTION OF KIDNEY TRANSPLANT REJECTION ·+2
AUROBINDO PHARM
Filter & compare in the drug finder → Opens the drug finder with Immunosuppressive Inosine Monophosphate Dehydrogenase Inhib. preselected. Add indication or manufacturer filters there.

About Immunosuppressive Inosine Monophosphate Dehydrogenase Inhib..

The class "Immunosuppressive Inosine Monophosphate Dehydrogenase Inhib." (or immunosuppressive inosine monophosphate dehydrogenase inhibitors) is a standard formulary classification for antiproliferative immunosuppressant agents, principally represented by mycophenolate mofetil and mycophenolic acid.

These medications function by reversibly and noncompetitively inhibiting inosine monophosphate dehydrogenase, the rate-limiting enzyme in de novo guanine nucleotide synthesis.

Because lymphocytes rely almost entirely on this de novo pathway rather than the purine salvage pathway, the resulting depletion of guanosine nucleotides selectively suppresses T- and B-cell proliferation and immune responses.

Clinically, these agents are primarily indicated for the prophylaxis of organ rejection in solid organ transplantation—such as kidney, heart, and liver allografts—and are widely utilized to manage severe autoimmune conditions, including lupus nephritis.