Regulatory Updates
FDA, EMA, TGA and global regulatory developments
Regulatory Updates
Sep 27, 2026•1 min read
FDA Approves Padagis Ciclopirox Olamine Suspension (ANDA077676)
FDA grants approval for ANDA077676, a prescription ciclopirox olamine 0.77% topical suspension from Padagis Israel Pharmaceuticals.
Regulatory Updates
Sep 27, 2026•1 min read
Sanofi-Aventis Canada Recalls Certain Insulin Pens and Cartridges Over Freezing Risk
Sanofi-Aventis Canada is recalling 1,043 insulin pens and cartridges from ~80 Canadian sites after they may have been frozen during shipping, potentially reducing effectiveness.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Approves Manufacturing Supplements for Sandoz Orphenadrine Citrate ER Tablet (ANDA 085046)
The FDA has approved several manufacturing (CMC) supplement submissions for Sandoz’s Orphenadrine Citrate extended‑release tablet (ANDA 085046), which is currently listed as discontinued.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Marks PANRAY's THEOLIXIR Oral Elixir as Discontinued (ANDA084559)
The FDA’s ANDA084559 filing shows PANRAY’s oral elixir THEOLIXIR, containing THEOPHYLLINE 80MG/15ML, is listed as discontinued.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Approves ANDA090137 for Sandoz Irinotecan Hydrochloride Injection
FDA approved Sandoz's ANDA090137 covering two Irinotecan Hydrochloride injectable products, both listed with discontinued marketing status.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Approves ANDA090468 for ZYFREL Oral Solution (Acetaminophen/Hydrocodone)
Cypress Pharm Inc.'s ZYFREL oral solution (acetaminophen 325 mg/15 mL and hydrocodone 7.5 mg/15 mL) received FDA approval under ANDA090468, with labeling supplements approved in 2016 and 2017.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Approves AstraZeneca ISOETHARINE Inhalation (ANDA089615)
The FDA approved ANDA089615 for ISOETHARINE HYDROCHLORIDE inhalation solution (0.125%) by AstraZeneca. The product is listed as discontinued.
Regulatory Updates
Sep 25, 2026•1 min read
Limited Number of Sarclisa Single-Use Vials Recalled in Nova Scotia Due to Possible Freezing
Health Canada recalls nine Sarclisa single-use vials from three Nova Scotia locations after possible freezing during shipment.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Approves ANDA079164 for Flecainide Acetate Tablets by Chartwell RX
The FDA approved the abbreviated new drug application ANDA079164 for Flecainide Acetate tablets (50 mg, 100 mg, 150 mg) from Chartwell RX, though the products are currently listed as discontinued.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Approves DIVALPROEX SODIUM (ANDA078853)
FDA grants approval for DIVALPROEX SODIUM tablets (ANDA078853) by Bionpharma Inc., with oral delayed‑release 125 mg, 250 mg and 500 mg equivalents.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Approves ANDA078547 for Nicotine Polacrilex OTC Chewing Gum
The FDA has approved ANDA078547 for a 2 mg nicotine polacrilex chewing gum, an over‑the‑counter nicotine replacement product marketed under several brand names.
Regulatory Updates
Sep 25, 2026•1 min read
FDA Approves Glenmark’s Carvedilol Generic Tablets (ANDA078251)
The FDA has granted labeling approval for Glenmark Pharmaceuticals’ generic carvedilol tablets (ANDA078251), available in 3.125 mg, 6.25 mg, 12.5 mg and 25 mg oral dosage forms.