CDER New: 6/17/2026

The approvals listed below may not be comprehensive. For the most current information, view the full listing of all approvals at Drugs@FDA.

What's New Related to Drugs

Updated Monday through Friday

  • Current and Resolved Drug Shortages and Discontinuations Reported to FDA
  • Drug Firm Annual Registration Status
  • Drug Firm Annual Registration Status Download File
  • National Drug Code Directory
  • NDC Unfinished Drugs Excluded Database File
  • NDC Database Excluded Packages and Products
  • Wholesale Distributor and Third-Party Logistics Providers Reporting
  • Drug Establishments Current Registration Site
  • Drugs@FDA Data Files 

Updated Biweekly

  • Competitive Generic Therapy Approvals

June 12, 2026

  • Orange Book
    • Approved Drug Products with Therapeutic Equivalence Evaluations
    • Orange Book Current Cumulative Supplement (updated)
    • Additions/Deletions for Prescription and OTC Drug Product Lists (updated)
    • Orange Book Data Files (compressed) (updated)
    • Reference Listed Drugs by ANDA Reference Standard List (updated)
    • Orange Book Patent Listing Dispute List (updated)
  • Draft Guidance: Forms FDA 3542a and FDA 3542: Questions and Answers
  • FDA approves belzutifan with pembrolizumab for adjuvant treatment of renal cell carcinoma
  • FDA approves capivasertib with abiraterone and prednisone for PTEN-deficient androgen pathway modulation-naïve or -sensitive prostate cancer
  • FDA Approves Drug for Pediatric Stage 3 Type I Diabetes

June 10, 2026

  • Public Notifications:
    • Business Pill may be harmful due to hidden drug ingredient
    • Branch Manager for Men may be harmful due to hidden drug ingredient
  • Webinar: ClinicalTrials.gov: Essentials for Academic Medical Centers
  • Drug Safety Communication: FDA Approves Labeling Changes for Over-the-Counter (OTC) Weight Loss Drug alli (Orlistat) to Warn of Risk of Kidney Stones and Kidney Injury

This report displays final approvals and tentative approvals of original and supplemental applications for the two days beginning on the earliest date listed below. Some approvals may be added to the Drugs@FDA database after this time span. For comprehensive approval reports, please use the monthly "All Approvals" report on Drugs@FDA.

June 16, 2026

Drug Name and
Application Number
Active Ingredient Dosage Form/ Route Submission Company Submission Classification Submission Status
Argatroban
NDA #020883
Argatroban Injectable; Injection SUPPL-21 Sandoz Labeling Approved
Rextovy
NDA #208969
Naloxone Hydrochloride Spray, Metered; Nasal SUPPL-2 Amphastar Pharms Inc Efficacy Approved
Isotretinoin
ANDA #213571
Isotretinoin Capsule; Oral SUPPL-11 Upsher Smith Labs Labeling Approved
Aprepitant
NDA #218754
Aprepitant Injectable; Intravenous ORIG-1 Azurity Type 5 - New Formulation or New Manufacturer Approved

June 15, 2026

Drug Name and
Application Number
Active Ingredient Dosage Form/ Route Submission Company Submission Classification Submission Status
Topiramate
ANDA #078499
Topiramate Tablet; Oral SUPPL-9 Aiping Pharm Inc Labeling Approved
Lenalidomide
ANDA #201452
Lenalidomide Capsule; Oral SUPPL-3 Arrow Intl Labeling Approved
Lenalidomide
ANDA #201452
Lenalidomide Capsule; Oral SUPPL-4 Arrow Intl Labeling Approved
Lenalidomide
ANDA #201452
Lenalidomide Capsule; Oral SUPPL-3 Arrow Intl Labeling Approved
Lenalidomide
ANDA #201452
Lenalidomide Capsule; Oral SUPPL-4 Arrow Intl Labeling Approved
Divalproex Sodium
ANDA #202419
Divalproex Sodium Tablet, Extended Release; Oral SUPPL-32 Aurobindo Pharma Ltd Labeling Approved
Divalproex Sodium
ANDA #202419
Divalproex Sodium Tablet, Extended Release; Oral SUPPL-33 Aurobindo Pharma Ltd Labeling Approved
Divalproex Sodium
ANDA #202419
Divalproex Sodium Tablet, Extended Release; Oral SUPPL-32 Aurobindo Pharma Ltd Labeling Approved
Divalproex Sodium
ANDA #202419
Divalproex Sodium Tablet, Extended Release; Oral SUPPL-33 Aurobindo Pharma Ltd Labeling Approved
Liraglutide
ANDA #213155
Liraglutide Solution; Subcutaneous ORIG-1 Mylan Institutional   Approved
Pantoprazole Sodium
ANDA #215860
Pantoprazole Sodium Injectable; Intravenous SUPPL-6 Meitheal Labeling Approved
Pantoprazole Sodium
ANDA #215860
Pantoprazole Sodium Injectable; Intravenous SUPPL-6 Meitheal Labeling Approved
Pantoprazole Sodium
ANDA #215860
Pantoprazole Sodium Injectable; Intravenous SUPPL-7 Meitheal Labeling Approved
Lacosamide
ANDA #217596
Lacosamide Solution; Oral ORIG-1 Prod Development   Approved
Perampanel
ANDA #219052
Perampanel Suspension; Oral ORIG-1 Taro   Approved
Cabergoline
ANDA #220309
Cabergoline Tablet; Oral ORIG-1 Renata   Approved
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