FDA has approved Aurobindo’s entacapone tablets USP, 200 mg, the generic equivalent to Novartis’ Comtan tablets 200 mg.
FDA has approved Aurobindo’s entacapone tablets USP, 200 mg, the generic equivalent to Novartis’ Comtan tablets 200 mg.
Entacapone is a commonly used drug in the treatment of Parkinson’s disease, especially in moderate to advanced stages.
Related: 4 ways the FAST Generics Act will help healthcare
Dr Hung“Taken with carbidopa/levodopa either as a separate pill or in combination, entacapone is effective in reducing ‘off’ time that can occur at later stages of disease,” Albert Hung, MD, director of the MGH National Parkinson Foundation Center of Excellence and assistant professor of neurology at Harvard Medical School, told FormularyWatch.
“Some patients may have difficulty obtaining entacapone due to cost; this approval will be a helpful step if it makes the medication more readily available, especially to those with less insurance coverage,” Dr Hung said.
Related:Study: Reduce long-term care use among patients with Parkinson's disease psychosis
Formulary managers will need to consider whether to carry combined carbidopa/levodopa/entacapone (currently branded as Stalevo), which offers convenience to taking the medications separately, versus requiring separate prescriptions for generic carbidopa/levodopa and entacapone, according to Dr Hung.
“As entacapone is already clinically available and used regularly, this approval may not affect prescribing patterns as much as it will the way the formularies and pharmacies fill the prescription,” he said. “If this new generic formulation is equally effective to the current forms, the use is likely to depend more on pharmacy/insurance choices than on neurologists/physicians.”
Entacapone has an estimated market size of $59 million for the 12 months ending April 2015 according to IMS.
Read next: FDA moves forward with generic Abilify from 4 different manufacturers despite Otsuka pushback
Navitus to Offer Unbranded Stelara Biosimilar, Remove Stelara from Formulary
March 13th 2025Lumicera Health Services, Navitus’ specialty pharmacy, has made a deal with Teva to offer an unbranded biosimilar that they estimate will save $112,000 and $336,000 per patient per year. Navitus will remove Stelara from formulary on July 1, 2025.
Read More
FDA Approves Neffy 1 mg Nasal Spray for Pediatric Patients
March 6th 2025Neffy 1 mg is now approved by the FDA to treat pediatric patients who weigh 33 to 65 lbs. Neffy was first FDA-approved as a 2 mg dose in August 2024 for the emergency treatment of anaphylaxis in children and adults weighing at least 66 lbs.
Read More