mye-koe-FEE-noe-late MOE-fe-til

mycophenolic acid: mye-koe-FEE-noe-lik

Mycophenolate mofetil:

• Prevention of rejection in allogeneic renal, hepatic, and cardiac transplantation (used concurrently with cyclosporine and corticosteroids).

Mycophenolic acid:

• Prevention of rejection in allogenic renal transplantation (used concurrently with cyclosporine and corticosteroids).

Unlabeled Use:

• Nephrotic syndrome.

• Inhibits the enzyme inosine monophosphate dehydrogenase, which is involved in purine synthesis. This inhibition results in suppression of T- and B-lymphocyte proliferation.

• Prevention of heart, kidney, or liver transplant rejection.

Absorption: Following oral and IV administration, mycophenolate mofetil is rapidly hydrolyzed to mycophenolic acid (MPA), the active metabolite. Absorption of enteric-coated mycophenolic acid (Myfortic) is delayed compared with mycophenolate mofetil (CellCept).

Distribution: Cross the placenta and enter breast milk.

Protein Binding: MPA — 97%.

Metabolism/Excretion: MPA is extensively metabolized; <1% excreted unchanged in urine. Some enterohepatic recirculation of MPA occurs.

Half-life: MPA — 8–18 hr.

Contraindicated in:

• Hypersensitivity
• Hypersensitivity to polysorbate 80 (for IV mycophenolate mofetil)
• OB: Pregnancy (↑ risk of congenital anomalies or spontaneous abortion).

Use Cautiously in:

• Active serious pathology of the GI tract (including history of ulcer disease or GI bleeding)
• Phenylketonuria (oral suspension contains aspartame)
• Severe chronic renal impairment (dose not to exceed 1 g twice daily (CellCept) if CCr <25 mL/min/1.73 m²); careful monitoring recommended
• Delayed graft function following transplantation (observe for ↑ toxicity)
• Lactation: Use while breastfeeding only if potential maternal benefit justifies potential risk to infant
• Rep: Women of reproductive potential and men with female partners of reproductive potential
• Pedi: Mycophenolate mofetil approved in children 3 mo for renal transplant; mycophenolic acid approved in children 5 yr for renal transplant; safety not established for other age groups
• Geri: ↑risk of adverse reactions related to immunosuppression in older adults.

CV: edema, hypertension, hypotension, tachycardia.

Derm: rash.

Endo: hypercholesterolemia, hyperglycemia, hyperkalemia, hypocalcemia, hypokalemia, hypomagnesemia.

GI: GI BLEEDING, anorexia, constipation, diarrhea, nausea, vomiting, abdominal pain.

GU: renal dysfunction.

Hemat: leukocytosis, leukopenia, thrombocytopenia, anemia, pure red cell aplasia.

Neuro: tremor, PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY (PML), anxiety, confusion, dizziness, headache, insomnia, paresthesia, sedation, tremor.

Resp: cough, dyspnea.

Misc: MALIGNANCY, fever, infection (including activation of latent viral infections such as Polyomavirus-associated nephropathy or Hepatitis B/C).

Drug-Drug:

• Combined use with azathioprine is not recommended (effects unknown).
• Acyclovir and ganciclovir compete with MPA for renal excretion and, in patients with renal dysfunction, may ↑ each other’s toxicity.
• Magnesium and aluminum hydroxide antacids ↓ the absorption of MPA (avoid simultaneous administration).
• Proton pump inhibitors, including dexlansoprazole, esomeprazole, lansoprazole, omeprazole, pantoprazole, and rabeprazole may ↓ levels
• Cholestyramine and colestipol↓ the absorption of MPA (avoid concurrent use).
• May ↓ the effectiveness of oral contraceptives (additional contraceptive method should be used).
• May ↓ the antibody response to and ↑ risk of adverse reactions from live attenuated vaccines.
• Amoxicillin/clavulanic acid or ciprofloxacin may ↓ MPA trough levels.
• Cyclosporine may ↓ levels; use caution when discontinuing cyclosporine (may ↑ mycophenolate levels) or when switching from cyclosporine to another immunosuppressant, such as tacrolimus or belatacept
• Telmisartan may ↓ levels

Mycophenolate Mofetil

• PO, IV (Adults): 1 g twice daily; IV should be started 24 hr after transplantation and switched to PO as soon as possible (IV not recommended for 14 days).
• PO (Children 3 mo–18 yr): 600 mg/m² twice daily (not to exceed 2 g/day).
Hepatic Transplantation
• PO, IV (Adults): 1 g twice daily IV, or 1.5 g twice daily PO. IV should be started 24 hr after transplantation and switched to PO as soon as possible (IV not recommended for 14 days).
Cardiac Transplantation
• PO, IV (Adults): 1.5 g twice daily; IV should be started 24 hr after transplantation and switched to PO as soon as possible (IV not recommended for 14 days).
Nephrotic Syndrome
• PO (Children): Frequent relapses — 12.5–18 mg/kg/dose twice daily; maximum: 2 g/day. Steroid-dependent — 12–18 mg/kg/dose or 600 mg/m² twice daily; maximum: 2 g/day.

Mycophenolic Acid

Mycophenolate mofetil and mycophenolic acid should not be used interchangeably without the advice of a health care professional.

• PO (Adults): 720 mg twice daily.
• PO (Children 5–16 yr and 1.19 m²): 400–450 mg/m² twice daily (not to exceed 720 mg twice daily).

• The initial dose of mycophenolate should be given within 24 hr of transplant.
  • Mycophenolate mofetil (Cellcept) and mycophenolic acid (Myfortic) are not interchangeable; rate of absorption is different.
• REMS: Mycophenolate is administered under REMS requirements. Prescribers are encouraged to complete Prescriber Training program and patients are encouraged to complete the Information for Patients to mitigate the risk of embryofetal toxicity associated with the use of mycophenolate during pregnancy.
• PO: Administer on an empty stomach, 1 hr before or 2 hr after meals. DNC: Swallow capsules and delayed-release tablets whole; do not open, crush, or chew. Mycophenolate may be teratogenic; wear gloves and avoid contact with skin or mucous membranes or inhalation of contents of capsules or oral suspension powder. Oral solution can be administered by nasogastric tube (minimum size of 8 French). Oral solution is stable for 60 days if refrigerated.
  • Do not administer mycophenolate concurrently with antacids containing magnesium or aluminum.

IV Administration:

• IV: IV route should only be used for patients unable to take oral medication and should be switched to oral dose form as soon as patient can tolerate capsules or tablets.
• Intermittent Infusion:
  Diluent: Reconstitute each vial with 14 mL of D5W. Shake gently to dissolve. Solution is slightly yellow; discard if solution is discolored or contains particulate matter. Dilute contents of 2 vials (1-g dose) further with 140 mL of D5W or 3 vials (1.5-g dose) with 210 mL of D5W.Concentration: 6 mg/mL. Solution is stable for 4 hr.
• Rate: Administer via slow IV infusion over at least 2 hr. Do not administer as a bolus or via rapid infusion; increases risk of phlebitis and thrombosis.
• Y-Site Compatibility:
  • alemtuzumab
  • alfentanil
  • amikacin
  • amiodarone
  • anidulafungin
  • argatroban
  • atracurium
  • bivalirudin
  • bumetanide
  • buprenorphine
  • butorphanol
  • calcium chloride
  • caspofungin
  • ceftolozane/tazobactam
  • chlorpromazine
  • ciprofloxacin
  • cisatracurium
  • daptomycin
  • dexmedetomidine
  • dexrazoxane
  • digoxin
  • diltiazem
  • diphenhydramine
  • dobutamine
  • dopamine
  • doxorubicin liposomal
  • doxycycline
  • droperidol
  • enalaprilat
  • ephedrine
  • epinephrine
  • erythromycin
  • esmolol
  • famotidine
  • fenoldopam
  • fentanyl
  • fluconazole
  • gentamicin
  • glycopyrrolate
  • granisetron
  • haloperidol
  • hydralazine
  • hydromorphone
  • insulin, regular
  • isavuconazonium
  • isoproterenol
  • labetalol
  • leucovorin calcium
  • levofloxacin
  • lidocaine
  • linezolid
  • lorazepam
  • magnesium sulfate
  • mannitol
  • meperidine
  • mesna
  • metoclopramide
  • metoprolol
  • metronidazole
  • midazolam
  • milrinone
  • minocycline
  • morphine
  • moxifloxacin
  • nalbuphine
  • naloxone
  • nicardipine
  • nitroglycerin
  • norepinephrine
  • 0.9% NaCl
  • octreotide
  • ondansetron
  • oxytocin
  • pamidronate
  • pancuronium
  • pentamidine
  • phentolamine
  • phenylephrine
  • potassium chloride
  • procainamide
  • prochlorperazine
  • promethazine
  • propranolol
  • quinupristin/dalfopristin
  • remifentanil
  • rocuronium
  • succinylcholine
  • sufentanil
  • tacrolimus
  • theophylline
  • tigecycline
  • tirofiban
  • tobramycin
  • vancomycin
  • vasopressin
  • vecuronium
  • verapamil
  • voriconazole
  • zidovudine
  • zoledronic acid
• Y-Site Incompatibility:
  • acyclovir
  • allopurinol
  • amifostine
  • aminocaproic acid
  • aminophylline
  • amphotericin B deoxycholate
  • amphotericin B lipid complex
  • amphotericin B liposome
  • ampicillin
  • ampicillin/sulbactam
  • azithromycin
  • aztreonam
  • calcium gluconate
  • cangrelor
  • cefazolin
  • cefotaxime
  • cefotetan
  • cefoxitin
  • ceftazidime
  • ceftriaxone
  • cefuroxime
  • chloramphenicol
  • clindamycin
  • dantrolene
  • defibrotide
  • dexamethasone
  • diazepam
  • eptifibatide
  • foscarnet
  • fosphenytoin
  • furosemide
  • ganciclovir
  • gemtuzumab ozogamicin
  • heparin
  • hydrocortisone
  • imipenem/cilastatin
  • ketorolac
  • meropenem
  • methotrexate
  • methylprednisolone
  • micafungin
  • nafcillin
  • nitroprusside
  • pantoprazole
  • pentobarbital
  • phenobarbital
  • phenytoin
  • piperacillin/tazobacatam
  • potassium acetate
  • potassium phosphates
  • sodium acetate
  • sodium bicarbonate
  • sodium phosphates
  • trimethoprim/sulfamethoxazole
.

CellCept

mycophenolic acid: Myfortic

Therapeutic Classification: Immunosuppressant agents

(Generic available)

Mycophenolate Mofetil

• Tablets: 500 mg;
• Capsules: 250 mg;
• Oral suspension (fruit flavor): 200 mg/mL;
• Powder for injection : 500 mg/vial;

Mycophenolic Acid

• Delayed-release tablets: 180 mg; 360 mg;

(blood levels of MPA)

• Assess for symptoms of organ rejection throughout therapy.
• Assess for signs of PML (hemiparesis, apathy, confusion, cognitive deficiencies, and ataxia) periodically during therapy.

• Verify negative urine pregnancy test with a specificity of 25 mIU/mL immediately prior to beginning therapy and again 8–10 days later. Repeat pregnancy tests should be preformed during routine follow-up visits.
  • Monitor CBC with differential weekly during the 1st mo, twice monthly for the 2nd and 3rd mo of therapy, and then monthly during the 1st yr. Neutropenia occurs most frequently from 31–180 days post-transplant. If ANC is <1000/mm³, dose should be reduced or discontinued.
  • Monitor hepatic and renal status and electrolytes periodically during therapy. May cause ↑ alkaline phosphatase, AST, ALT, LDH, BUN, and serum creatinine. May also cause hyperkalemia, hypokalemia, hypocalcemia, hypomagnesemia, hyperglycemia, and hyperlipidemia.

• Instruct patient to take medication as directed, at the same time each day. Take missed dose as soon as remembered, but not if within 2 hrs before next dose. Do not skip or double up on missed doses. Do not discontinue without consulting health care professional. Advise patient to read Medication Guide before starting therapy and with each Rx refill in case of changes.
• REMS: Explain REMS program to patient.
• Reinforce the need for lifelong therapy to prevent transplant rejection. Review symptoms of rejection for the transplanted organ, and stress need to notify health care professional immediately if signs of rejection or infection occur.
• May cause somnolence, confusion, dizziness, tremor, or hypotension. Caution patient to avoid driving and other activities requiring alertness until response from medication is known.
• Instruct patient to notify health care professional immediately if signs and symptoms of infection (temperature 100.5°F, cold symptoms [runny nose, sore throat], flu symptoms [upset stomach, stomach pain, vomiting, diarrhea], earache or headache, pain during urination, frequent urination, white patches in mouth or throat, unexpected bruising or bleeding, cuts, scrapes, or incisions that are red, warm, and oozing pus) or PML.
• Advise patient to avoid contact with persons with contagious diseases.
• Advise patient to avoid vaccinations with live attenuated virus during therapy.
• Inform patient of the increased risk of lymphoma and other malignancies. Advise patient to use sunscreen and wear protective clothing to decrease risk of skin cancer.
• Advise patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and to consult with health care professional before taking other medications.
• Instruct patient to avoid donating blood during and for at least 6 wk after discontinuation of therapy.
• Rep: Inform females of reproductive potential of the potential for pregnancy loss and fetal harm. Discuss importance of simultaneously using two reliable nonhormonal forms of contraception, unless abstinence is the chosen method, prior to beginning, during, and for 6 wk following discontinuation of therapy and to avoid breast feeding. Discuss acceptable forms of contraception with health care professional. Mycophenolate may decrease effectiveness of hormonal contraceptives. Encourage patients who become pregnant during or within 6 wk after therapy to enroll in the Pregnancy Registry by calling 1-800-617-8191 or to monitor pregnancy outcomes in women exposed to mycophenolate during pregnancy. Instruct male patients with female partners of reproductive potential to use effective contraception during and for at least 90 days after discontinuing therapy. Advise male patients to avoid semen donation during and for at least 90 days after discontinuing therapy.
• Emphasize the importance of routine follow-up laboratory tests.

• Prevention of rejection of transplanted organs.

NDC Code^*

• 0004- Genentech, Inc.
  • 0004-0259- CellCept
    • 0004-0259-01- 1 BOTTLE, PLASTIC in 1 CARTON (0004-0259-01) > 100 CAPSULE in 1 BOTTLE, PLASTIC

• 0004- Genentech, Inc.
  • 0004-0259- CellCept
    • 0004-0259-43- 1 BOTTLE, PLASTIC in 1 CARTON (0004-0259-43) > 500 CAPSULE in 1 BOTTLE, PLASTIC

• 0004- Genentech, Inc.
  • 0004-0260- CellCept
    • 0004-0260-01- 1 BOTTLE, PLASTIC in 1 CARTON (0004-0260-01) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

• 0004- Genentech, Inc.
  • 0004-0260- CellCept
    • 0004-0260-43- 1 BOTTLE, PLASTIC in 1 CARTON (0004-0260-43) > 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

• 0004- Genentech, Inc.
  • 0004-0261- CellCept
    • 0004-0261-29- 1 BOTTLE, PLASTIC in 1 CARTON (0004-0261-29) > 225 mL in 1 BOTTLE, PLASTIC

• 0004- Genentech, Inc.
  • 0004-0298- CellCept
    • 0004-0298-09- 4 VIAL in 1 CARTON (0004-0298-09) > 20 mL in 1 VIAL

• 0054- West-Ward Pharmaceuticals Corp
  • 0054-0163- Mycophenolate Mofetil
    • 0054-0163-25- 100 CAPSULE in 1 BOTTLE (0054-0163-25)

• 0054- West-Ward Pharmaceuticals Corp
  • 0054-0163- Mycophenolate Mofetil
    • 0054-0163-29- 500 CAPSULE in 1 BOTTLE (0054-0163-29)

• 0054- West-Ward Pharmaceuticals Corp
  • 0054-0166- Mycophenolate Mofetil
    • 0054-0166-25- 100 TABLET in 1 BOTTLE (0054-0166-25)

• 0054- West-Ward Pharmaceuticals Corp
  • 0054-0166- Mycophenolate Mofetil
    • 0054-0166-29- 500 TABLET in 1 BOTTLE (0054-0166-29)

• 0093- Teva Pharmaceuticals USA, Inc.
  • 0093-7334- Mycophenolate Mofetil
    • 0093-7334-01- 100 CAPSULE in 1 BOTTLE (0093-7334-01)

• 0093- Teva Pharmaceuticals USA, Inc.
  • 0093-7334- Mycophenolate Mofetil
    • 0093-7334-05- 500 CAPSULE in 1 BOTTLE (0093-7334-05)

• 0378- Mylan Pharmaceuticals Inc.
  • 0378-2250- Mycophenolate Mofetil
    • 0378-2250-01- 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2250-01)

• 0378- Mylan Pharmaceuticals Inc.
  • 0378-2250- Mycophenolate Mofetil
    • 0378-2250-05- 500 CAPSULE in 1 BOTTLE, PLASTIC (0378-2250-05)

• 0378- Mylan Pharmaceuticals Inc.
  • 0378-4472- Mycophenolate Mofetil
    • 0378-4472-01- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4472-01)

• 0378- Mylan Pharmaceuticals Inc.
  • 0378-4472- Mycophenolate Mofetil
    • 0378-4472-05- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4472-05)

• 0781- Sandoz Inc
  • 0781-2067- Mycophenolate Mofetil
    • 0781-2067-01- 100 CAPSULE in 1 BOTTLE (0781-2067-01)

• 0781- Sandoz Inc
  • 0781-2067- Mycophenolate Mofetil
    • 0781-2067-05- 500 CAPSULE in 1 BOTTLE (0781-2067-05)

• 0781- Sandoz Inc
  • 0781-2067- Mycophenolate Mofetil
    • 0781-2067-72- 120 CAPSULE in 1 BOTTLE (0781-2067-72)

• 0781- Sandoz Inc
  • 0781-2067- Mycophenolate Mofetil
    • 0781-2067-89- 12 CAPSULE in 1 CARTON (0781-2067-89)

• 0781- Sandoz Inc
  • 0781-5175- Mycophenolate Mofetil
    • 0781-5175-01- 100 TABLET, FILM COATED in 1 BOTTLE (0781-5175-01)

• 0781- Sandoz Inc
  • 0781-5175- Mycophenolate Mofetil
    • 0781-5175-05- 500 TABLET, FILM COATED in 1 BOTTLE (0781-5175-05)

• 0781- Sandoz Inc
  • 0781-5175- Mycophenolate Mofetil
    • 0781-5175-10- 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5175-10)

• 16729- Accord Healthcare Inc.
  • 16729-019- mycophenolate mofetil
    • 16729-019-01- 100 TABLET in 1 BOTTLE (16729-019-01)

• 16729- Accord Healthcare Inc.
  • 16729-019- mycophenolate mofetil
    • 16729-019-16- 500 TABLET in 1 BOTTLE (16729-019-16)

• 16729- Accord Healthcare Inc.
  • 16729-094- mycophenolate mofetil
    • 16729-094-01- 100 CAPSULE in 1 BOTTLE (16729-094-01)

• 16729- Accord Healthcare Inc.
  • 16729-094- mycophenolate mofetil
    • 16729-094-16- 500 CAPSULE in 1 BOTTLE (16729-094-16)

• 17478- Akorn, Inc.
  • 17478-422- Mycophenolate Mofetil
    • 17478-422-40- 4 VIAL in 1 CARTON (17478-422-40) > 20 mL in 1 VIAL

• 17478- Akorn, Inc.
  • 17478-957- Mycophenolate Mofetil
    • 17478-957-40- 4 VIAL in 1 CARTON (17478-957-40) > 20 mL in 1 VIAL

• 42023- Par Pharmaceutical, Inc.
  • 42023-172- Mycophenolate Mofetil
    • 42023-172-04- 4 VIAL in 1 CARTON (42023-172-04) > 20 mL in 1 VIAL

• 50090- A-S Medication Solutions
  • 50090-2246- Mycophenolate mofetil
    • 50090-2246-0- 180 TABLET, FILM COATED in 1 BOTTLE (50090-2246-0)

• 50090- A-S Medication Solutions
  • 50090-2541- mycophenolate mofetil
    • 50090-2541-0- 180 TABLET in 1 BOTTLE (50090-2541-0)

• 50090- A-S Medication Solutions
  • 50090-4275- Mycophenolate Mofetil
    • 50090-4275-0- 180 TABLET, FILM COATED in 1 BOTTLE (50090-4275-0)

• 51079- Mylan Institutional Inc.
  • 51079-379- Mycophenolate Mofetil
    • 51079-379-20- 100 BLISTER PACK in 1 CARTON (51079-379-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-379-01)

• 51079- Mylan Institutional Inc.
  • 51079-721- Mycophenolate Mofetil
    • 51079-721-20- 100 BLISTER PACK in 1 CARTON (51079-721-20) > 1 CAPSULE in 1 BLISTER PACK (51079-721-01)

• 55154- Cardinal Health
  • 55154-5382- Mycophenolate Mofetil
    • 55154-5382-0- 10 BLISTER PACK in 1 BAG (55154-5382-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

• 55154- Cardinal Health
  • 55154-6262- Mycophenolate Mofetil
    • 55154-6262-0- 10 BLISTER PACK in 1 BAG (55154-6262-0) > 1 CAPSULE in 1 BLISTER PACK

• 60429- Golden State Medical Supply, Inc.
  • 60429-059- Mycophenolate Mofetil
    • 60429-059-01- 100 CAPSULE in 1 BOTTLE, PLASTIC (60429-059-01)

• 60429- Golden State Medical Supply, Inc.
  • 60429-059- Mycophenolate Mofetil
    • 60429-059-05- 500 CAPSULE in 1 BOTTLE, PLASTIC (60429-059-05)

• 60429- Golden State Medical Supply, Inc.
  • 60429-070- Mycophenolate Mofetil
    • 60429-070-01- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60429-070-01)

• 60429- Golden State Medical Supply, Inc.
  • 60429-070- Mycophenolate Mofetil
    • 60429-070-05- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60429-070-05)

• 60687- American Health Packaging
  • 60687-427- Mycophenolate Mofetil
    • 60687-427-01- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-427-01) > 1 CAPSULE in 1 BLISTER PACK (60687-427-11)

• 60687- American Health Packaging
  • 60687-438- Mycophenolate mofetil
    • 60687-438-01- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-438-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-438-11)

• 64380- Strides Pharma Science Limited
  • 64380-725- Mycophenolate mofetil
    • 64380-725-06- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-725-06)

• 64380- Strides Pharma Science Limited
  • 64380-725- Mycophenolate mofetil
    • 64380-725-07- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-725-07)

• 64380- Strides Pharma Science Limited
  • 64380-726- Mycophenolate mofetil
    • 64380-726-06- 100 CAPSULE in 1 BOTTLE, PLASTIC (64380-726-06)

• 64380- Strides Pharma Science Limited
  • 64380-726- Mycophenolate mofetil
    • 64380-726-07- 500 CAPSULE in 1 BOTTLE, PLASTIC (64380-726-07)

• 64380- Strides Pharma Science Limited
  • 64380-726- Mycophenolate mofetil
    • 64380-726-11- 120 CAPSULE in 1 BOTTLE, PLASTIC (64380-726-11)

• 66689- VistaPharm, Inc.
  • 66689-307- Mycophenolate Mofetil
    • 66689-307-08- 1 BOTTLE, PLASTIC in 1 CARTON (66689-307-08) > 250 mL in 1 BOTTLE, PLASTIC

• 67877- Ascend Laboratories, LLC
  • 67877-225- Mycophenolate Mofetil
    • 67877-225-01- 100 TABLET, FILM COATED in 1 BOTTLE (67877-225-01)

• 67877- Ascend Laboratories, LLC
  • 67877-225- Mycophenolate Mofetil
    • 67877-225-05- 500 TABLET, FILM COATED in 1 BOTTLE (67877-225-05)

• 67877- Ascend Laboratories, LLC
  • 67877-225- Mycophenolate Mofetil
    • 67877-225-38- 10 BLISTER PACK in 1 CARTON (67877-225-38) > 10 TABLET, FILM COATED in 1 BLISTER PACK

• 67877- Ascend Laboratories, LLC
  • 67877-225- Mycophenolate Mofetil
    • 67877-225-84- 3 BLISTER PACK in 1 CARTON (67877-225-84) > 10 TABLET, FILM COATED in 1 BLISTER PACK

• 67877- Ascend Laboratories, LLC
  • 67877-230- Mycophenolate mofetil
    • 67877-230-22- 1 BOTTLE, PLASTIC in 1 CARTON (67877-230-22) > 225 mL in 1 BOTTLE, PLASTIC

• 67877- Ascend Laboratories, LLC
  • 67877-266- mycophenolate mofetil
    • 67877-266-01- 100 CAPSULE in 1 BOTTLE (67877-266-01)

• 67877- Ascend Laboratories, LLC
  • 67877-266- mycophenolate mofetil
    • 67877-266-05- 500 CAPSULE in 1 BOTTLE (67877-266-05)

• 67877- Ascend Laboratories, LLC
  • 67877-266- mycophenolate mofetil
    • 67877-266-38- 10 BLISTER PACK in 1 CARTON (67877-266-38) > 10 CAPSULE in 1 BLISTER PACK

• 67877- Ascend Laboratories, LLC
  • 67877-266- mycophenolate mofetil
    • 67877-266-84- 3 BLISTER PACK in 1 CARTON (67877-266-84) > 10 CAPSULE in 1 BLISTER PACK

• 68084- American Health Packaging
  • 68084-795- Mycophenolate Mofetil
    • 68084-795-01- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-795-01) > 1 CAPSULE in 1 BLISTER PACK (68084-795-11)

• 68084- American Health Packaging
  • 68084-801- Mycophenolate mofetil
    • 68084-801-01- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-801-01) > 1 TABLET in 1 BLISTER PACK (68084-801-11)

• 68254- CONCORD BIOTECH LIMITED
  • 68254-5000- MYCOPHENOLATE MOFETIL
    • 68254-5000-1- 100 CAPSULE in 1 BOTTLE (68254-5000-1)

• 68254- CONCORD BIOTECH LIMITED
  • 68254-5000- MYCOPHENOLATE MOFETIL
    • 68254-5000-2- 500 CAPSULE in 1 BOTTLE (68254-5000-2)

• 68382- Zydus Pharmaceuticals (USA) Inc.
  • 68382-669- Mycophenolate Mofetil
    • 68382-669-08- 4 VIAL in 1 CARTON (68382-669-08) > 20 mL in 1 VIAL

• 70748- Lupin Pharmaceuticals, Inc.
  • 70748-186- MYCOPHENOLATE MOFETIL
    • 70748-186-01- 100 CAPSULE in 1 BOTTLE (70748-186-01)

• 70748- Lupin Pharmaceuticals, Inc.
  • 70748-186- MYCOPHENOLATE MOFETIL
    • 70748-186-02- 500 CAPSULE in 1 BOTTLE (70748-186-02)

• 70771- Cadila Healthcare Limited
  • 70771-1084- Mycophenolate Mofetil
    • 70771-1084-8- 4 VIAL in 1 CARTON (70771-1084-8) > 20 mL in 1 VIAL

• 71610- Aphena Pharma Solutions - Tennessee, LLC
  • 71610-033- Mycophenolate Mofetil
    • 71610-033-70- 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-70)