Mylan Recalls One Batch of Insulin Glargine
Some vials have been found to be missing a label.
Mylan Pharmaceuticals, a Viatris company, is recalling one batch of its insulin glargine (insulin glargine- yfgn) injection, 100 units/mL (U-100), which is packaged in a 10 mL vial that is inside a carton. The product being recalled is not the branded Semglee vial but the unbranded insulin glargine- yfgn vial.
This batch is being recalled due to the potential for the label to be missing on some vials but the product information, batch number and expiration date are on the carton.
This batch was manufactured by Biocon Sdn. Bhd. and was distributed in the United State by Mylan Specialty between December 9, 2021, and March 4, 2022.
The impacted product has an expiration date of August 2023, with an NDC number of 49502-393-80.
Mylan notes that a missing label could lead to a mix-up of products/strengths, which may result in less optimal glycemic control. To date, no adverse events related to this recall have been received for this product.
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
