We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
  • SKIP TO CONTENT
  • SKIP NAVIGATION
  • Drug News
    • Trending
    • Commercial Operations
    • GMPs, Inspections and Audits
    • Postmarket Safety
    • Quality
    • Regulatory Affairs
    • Research and Development
    • Submissions and Approvals
    • FDAnews Drug Daily Bulletin
    • Drug Industry Daily
  • Device News
    • Trending
    • Commercial Operations
    • Inspections and Audits
    • Postmarket Safety
    • Quality
    • Regulatory Affairs
    • Research and Development
    • Submissions and Approvals
    • FDAnews Device Daily Bulletin
    • FDAnews Device Daily Bulletin Premium
  • Books
    • FDAnews Books Library
    • Drug Books
    • Device Books
  • Training/Events
    • Webinar Training Pass
    • Events
  • Resources
    • Form 483s Database
    • FDA Approved Drugs
    • eCFR and Guidances
    • White Papers
  • CenterWatch
  • About Us
    • The Company
    • Contact Us
  • Advertising
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » FDA Revokes Ranbaxy ANDAs for Generic Nexium, Valcyte

FDA Revokes Ranbaxy ANDAs for Generic Nexium, Valcyte

November 24, 2014

Citing quality problems at two of Ranbaxy’s Indian manufacturing facilities, the FDA has revoked its tentative approvals for two of the company’s ANDAs, one for a generic of AstraZeneca blockbuster Nexium and the other for Hoffman-LaRoche AIDS drug Valycte.

The move to revoke the ANDAs will cost Ranbaxy the 180 days of exclusivity it won as first filer for Valcyte (valganciclovir HCl). It immediately clears the way for two generics of the drug to go to market since both Endo and Dr. Reddy’s have already won approval for their ANDAs.

The picture surrounding Nexium (esomeprazole magnesium) is less clear. At least eight companies in addition to Ranbaxy have filed ANDAs against Nexium, but none have been approved. Ranbaxy had tentatively won 180-day exclusivity as first-filer against Nexium 20 mg and 40 mg capsules, and the company declined to say whether it had forfeited that exclusivity.

In announcing the FDA’s decision earlier this month, Ranbaxy said the agency told the company it had revoked its approvals, first granted in 2008, because the facilities referenced in the ANDAs were not in compliance with GMP requirements. Ranbaxy acknowledged losing exclusivity on Valycte, but not Nexium. Ranbaxy last week sued the FDA, seeking a restraining order on approval of other ANDAs for the drug.

AstraZeneca said it assumes there will be no generic competition to Nexium in the U.S. this year.

The FDA’s decision is just the latest move in Ranbaxy’s long-running battle to bring its version of the blockbuster heartburn drug to market. Under a settlement with AstraZeneca, Ranbaxy said it should have been able to launch generic Nexium by as early as May.

A consent agreement between Ranbaxy and the FDA had given the company until Sept. 30 to reach certain quality milestones before it risked losing exclusivity.

Further adding to the drama has been an ongoing lawsuit that says the 2008 settlement agreement between AstraZeneca and Ranbaxy, as well as separate settlements with other ANDA filers, constituted an illegal pay-for-delay deal putting off generic Nexium.

Don’t have approvals revoked over quality and GMP issues. Train your staff the right way with GMP Training for Drugmakers.

Drugs Submissions and Approvals

Upcoming Events

  • 04Apr

    Optimizing Quality Control Operations with Unified Quality

  • 20Apr

    Medical Device Enforcement: Latest Developments from the FDA, DOJ and FTC

  • 25Apr

    Effective Root Cause Analysis and CAPA Investigations for Drugs, Devices and Clinical Trials

  • 26Apr

    FDA’s New Laws and Regulations: What Drug and Biologics Manufacturers Need to Know

  • 27Apr

    Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis

  • 17May

    2023 WCG Avoca Quality Consortium Summit

Featured Products

  • FDA’s New Quality System Regulation: Transitioning from QSR to ISO 13485

    FDA’s New Quality System Regulation: Transitioning from QSR to ISO 13485

  • Selecting and Implementing Electronic Document Management Systems in the EU

    Selecting and Implementing Electronic Document Management Systems in the EU

Featured Stories

  • NVIDIA and Medtronic to Develop Artificial Intelligence Solutions

  • FDA Approves Evkeeza for Kids With Ultra-Rare Cholesterol Disorder

  • GrayMatters Health’s Digital Therapy Device for PTSD Cleared

  • Dupixent Shows Positive Results in COPD Study

The Revised ICH E8: A Guide to New Clinical Trial Requirements

Learn More
  • Drug Products
    • Quality
    • Regulatory Affairs
    • GMPs
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Device Products
    • Quality
    • Regulatory Affairs
    • QSR
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Clinical Products
    • Trial Design
    • Data Integrity
    • GCP
    • Inspections and Audits
    • Transparency
  • Privacy Policy
  • Do Not Sell or Share My Data
Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 703.538.7600 – Toll free 888.838.5578

Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing