Categories: Manufacturers (D)

Ranbaxy loses 180-day exclusivity for generic Nexium

Will pursue legal options to preserve its rights

Delhi, February, 2015

After losing the approval for manufacturing and selling esomeprazole magnesium delayed-release capsules (20 mg and 40 mg) in November, Ranbaxy Laboratories has now also lost the 180-days exclusivity for the medicine.

Generic versions

The drug-maker had received approval from the US Food and Drug Administration (FDA) to launch the first generic versions of AstraZeneca’s heartburn medicine Nexium (esomeprazole magnesium) in 2008.

However, in November 2014, the US regulator withdrew that nod, saying the original decision to grant tentative approval was an “error” since at that time the company’s facilities were under scrutiny.

Now, the FDA has informed the company that the six-month period of exclusivity for launching the generic equivalent of the medicine also stands cancelled.

Legal options

Ranbaxy said, on Tuesday, it will pursue “all available legal options to preserve its rights”.

In 2008, the year Ranbaxy got approval for esomeprazole magnesium, the company had received two warning letters and the US FDA had issued import alerts against its facilities in Dewas (Madhya Pradesh) and Poanta Sahib (Himachal Pradesh).

The company was under fire for violations of several good manufacturing practices, manufacturing adulterated drugs and other issues.

Along with the withdrawal of approval for esomeprazole magnesium, the US FDA had also rescinded its nod to Ranbaxy for making the generic version of Roche’s antiviral medicine, Valcyte (valganciclovir hydrochloride).

Later the regulator gave nod to Dr Reddy’s Laboratories and Endo Pharmaceuticals for manufacturing the generic versions of this medicine.

Restraining order

Ranbaxy had sued the US FDA over this issue in the DC Federal Court and requested the court to issue restraining order against the US regulator from giving its approval to other ANDAs (abbreviated new drug applications) for generic versions of both Valcyte and Nexium.

The US court, however, refused to block the regulator from granting such approvals.

The Pharma Times News Bureau

Recent Posts

8 Ways Insomnia Affects Skin Health & How To Avoid It

By Dr. Priyanka Kuri, Consultant - Dermatology, Aster Whitefield Hospital, Bengaluru Insomnia, the persistent inability…

1 day ago

Breaking New Ground in Migraine Care: A Landmark Session on Diagnosis and Treatment

Illuminating Latest Advances in Migraine Diagnosis and Treatment New Delhi, December 21, 2024: In a…

1 day ago

Healthcare Startups to Watch Out for in 2025

New Delhi, December 20, 2024: The healthcare sector is undergoing a transformation fueled by technological…

2 days ago

DKMS’s First Global Impact Report of 2023 Serves as New Ray of Hope for Blood Cancer Patients Worldwide

National, December 20, 2024: DKMS just published its first Global Impact Report that outlines the organization's…

2 days ago

Sterling Biotech to start world’s first precision fermentation-based dairy protein factory in Gujarat

Ahmedabad, December 19, 2024: Sterling Biotech Limited, a joint venture between Perfect Day and Zydus, has…

3 days ago

Pioneers in Senior Care, Antara, Partners with Leading Diagnostics Player Dr. Lal PathLabs to Strengthen its Geriatric Care Services

New Delhi, December 19, 2024: Antara Senior Care, an integrated eco-system provider for lifestyle and…

3 days ago