CDER New: 5/12/2026

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

May 11, 2026

  • CDER Statement: FDA Alerts Health Care Providers and Patients about Increased Risk of New Blood Cancers with Tazverik (tazemetostat) Use; Sponsor to Voluntarily Withdraw Product from Market
  • Workshop: Advancing Generic Drug Development: Bioequivalence Challenges for Patient-Centric Oral Formulations

May 8, 2026

  • FDA approves zenocutuzumab-zbco for advanced, unresectable or metastatic cholangiocarcinoma
  • 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)
  • Final guidance: Postapproval Pregnancy Safety Studies
  • Final guidance: Pulmonary Tuberculosis: Developing Drugs for Treatment
  • Final guidance: Clostridioides difficile Infection: Developing Drugs for Treatment, Reduction of Recurrence, and Prevention

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.

May 8, 2026

Drug Name and
Application Number
Active Ingredient Dosage Form/ Route Submission Company Submission Classification Submission Status
Adempas
NDA #204819
Riociguat Tablet; Oral SUPPL-20 Bayer Hlthcare REMS Approved
Adempas
NDA #204819
Riociguat Tablet; Oral SUPPL-20 Bayer Hlthcare REMS Approved
Riociguat
ANDA #211135
Riociguat Tablet; Oral SUPPL-1 Msn REMS Approved
Nurtec Odt
NDA #212728
Rimegepant Sulfate Tablet, Orally Disintegrating; Oral SUPPL-32 Pfizer Labeling Approved
Carbidopa and Levodopa
ANDA #216537
Carbidopa; Levodopa Tablet; Oral SUPPL-2 Aurobindo Pharma Ltd Labeling Approved
Levetiracetam In Sodium Chloride
ANDA #218364
Levetiracetam Injectable; Intravenous ORIG-1 Mylan Labs Ltd   Approved
Sdamlo
NDA #219531
Amlodipine Besylate For Solution; Oral SUPPL-2 Brillian Pharma Labeling Approved
Ocrevus
BLA #761053
Ocrelizumab Injectable; Injection SUPPL-38 Genentech Inc Efficacy Approved
Vyvgart
BLA #761195
Efgartigimod Alfa Injectable; Injection SUPPL-16 Argenx Bv Efficacy Approved
Vyvgart Hytrulo
BLA #761304
Efgartigimod Alfa and Hyaluronidase-Qvfc Injectable; Injection SUPPL-18 Argenx Bv Efficacy Approved
Bizengri
BLA #761352
Zenocutuzumab-Zbco Injection; Solution SUPPL-10 Merus N.V. Efficacy Approved

May 7, 2026

Drug Name and
Application Number
Active Ingredient Dosage Form/ Route Submission Company Submission Classification Submission Status
Altace
NDA #019901
Ramipril Capsule; Oral SUPPL-72 King Pharms Llc Labeling Approved
Zyprexa Relprevv
NDA #022173
Olanzapine Pamoate Suspension, Extended Release; Intramuscular SUPPL-43 Cheplapharm Labeling Approved
Zyprexa Relprevv
NDA #022173
Olanzapine Pamoate Suspension, Extended Release; Intramuscular SUPPL-43 Cheplapharm Labeling Approved
Zyprexa Relprevv
NDA #022173
Olanzapine Pamoate Suspension, Extended Release; Intramuscular SUPPL-43 Cheplapharm Labeling Approved
Zyprexa Relprevv
NDA #022173
Olanzapine Pamoate Suspension, Extended Release; Intramuscular SUPPL-40 Cheplapharm REMS Approved
Brilinta
NDA #022433
Ticagrelor Tablet; Oral SUPPL-39 Astrazeneca Labeling Approved
Gabapentin
ANDA #075435
Gabapentin Capsule; Oral SUPPL-30 Teva Pharms Labeling Approved
Gabapentin
ANDA #075435
Gabapentin Capsule; Oral SUPPL-29 Teva Pharms Labeling Approved
Gabapentin
ANDA #075435
Gabapentin Capsule; Oral SUPPL-30 Teva Pharms Labeling Approved
Risperidone
ANDA #076228
Risperidone Tablet; Oral SUPPL-20 Heritage Pharma Avet Labeling Approved
Risperidone
ANDA #076228
Risperidone Tablet; Oral SUPPL-21 Heritage Pharma Avet Labeling Approved
Losartan Potassium
ANDA #076958
Losartan Potassium Tablet; Oral SUPPL-19 Teva Labeling Approved
Losartan Potassium
ANDA #076958
Losartan Potassium Tablet; Oral SUPPL-19 Teva Labeling Approved
Sertraline Hydrochloride
ANDA #077663
Sertraline Hydrochloride Tablet; Oral SUPPL-9 Heritage Pharma Avet Labeling Approved
Sertraline Hydrochloride
ANDA #077663
Sertraline Hydrochloride Tablet; Oral SUPPL-9 Heritage Pharma Avet Labeling Approved
Alendronate Sodium
ANDA #077982
Alendronate Sodium Tablet; Oral SUPPL-13 Apotex Labeling Approved
Acetazolamide Sodium
ANDA #200880
Acetazolamide Sodium Injectable; Injection SUPPL-15 Mylan Asi Labeling Approved
Sodium Thiosulfate
NDA #203923
Sodium Thiosulfate Solution; Intravenous SUPPL-5 Hope Pharms Manufacturing (CMC) Approved
Sodium Thiosulfate
NDA #203923
Sodium Thiosulfate Solution; Intravenous SUPPL-5 Hope Pharms Manufacturing (CMC) Approved
Mekinist
NDA #204114
Trametinib Dimethyl Sulfoxide Tablet; Oral SUPPL-42 Novartis Labeling Approved
Capecitabine
ANDA #204345
Capecitabine Tablet; Oral SUPPL-5 Dr Reddys Labeling Approved
Capecitabine
ANDA #204345
Capecitabine Tablet; Oral SUPPL-5 Dr Reddys Labeling Approved
Capecitabine
ANDA #204741
Capecitabine Tablet; Oral SUPPL-13 Amneal Pharms Labeling Approved
Paliperidone
ANDA #205402
Paliperidone Tablet, Extended Release; Oral ORIG-1 I3 Pharms   Approved
Empagliflozin
ANDA #212336
Empagliflozin Unknown ORIG-1 Dr Reddys Labs Ltd   Tentative Approval
Hydrocortisone Sodium Succinate
ANDA #217191
Hydrocortisone Sodium Succinate Injectable; Injection ORIG-1 Zydus Pharms   Approved
Atropine Sulfate
ANDA #218148
Atropine Sulfate Solution/Drops; Ophthalmic SUPPL-6 Mankind Pharma Labeling Approved
Brimonidine Tartrate
ANDA #218558
Brimonidine Tartrate Solution/Drops; Ophthalmic ORIG-1 Micro Labs   Approved
Siliq
BLA #761032
Brodalumab Injectable; Injection SUPPL-21 Valeant Luxembourg REMS Approved
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