Levonorgestrel and ethinyl estradiol tablets, 0.15/0.03 mg (equiv to Seasonale tablets)
Levonorgestrel and ethinyl estradiol tablets, 0.15/0.03 mg (equiv to Seasonale tablets)
WATSON
Topiramate tablets, 25, 100, and 200 mg (equiv to Topamax tablets)
Diltiazem extended-release capsules, 120, 180, 240, 300, 360, and 420 mg (equiv to Tiazac extended-release capsules)
KV PHARMACEUTICAL
Prednicarbate cream, 0.1% (emollient) (equiv to Dermatop emollient cream, 0.1%)
ALTANA
Caffeine citrate injection, 20 mg/mL, packaged in 60 mg/3 mL single-dose vials (equiv to Cafcit injection)
PHARMAFORCE
Caffeine citrate oral solution, 20 mg/mL, packaged in 60 mg/3 mL vials (equiv to Cafcit oral solution)
PHARMAFORCE
Balanced salt solution (sterile irrigation solution) (equiv to BSS sterile irrigating solution)
AKORN
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.
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David Calabrese of OptumRx Talks Top Three Drugs in Pipeline, Industry Trends in Q2
July 1st 2020In this week's episode of Tuning Into The C-Suite podcast, MHE's Briana Contreras chatted with David Calabrese, R.Ph, MHP, who is senior vice president and chief pharmacy officer of pharmacy care services company, OptumRx. David is also a member of Managed Healthcare Executives’ Editorial Advisory Board. During the discussion, he shared the OptumRx Quarter 2 Drug Pipeline Insights Report of 2020. Some of the information shared includes the three notable drugs currently being reviewed or those that have been recently approved by the FDA. Also discussed were any interesting industry trends to watch for.
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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.
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