Lupin said the US drug regulator has classified its inspection of the Pithampur Unit 2 manufacturing facility as 'official action indicated' (OAI).

The US Food and Drug Administration (USFDA) had conducted inspections at the facility from July 8 to July 17, 2025, and closed it by issuing Form 483 with four observations.
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CNBC TV1830-12-2025, 17:35

Lupin's VISUfarma Acquisition Pushed to Feb 2026; Fortifies Diabetes & Obesity Segment

  • Lupin's acquisition of Amsterdam-based VISUfarma BV is now expected to close by February 28, 2026, delayed from the earlier target of end-2025.
  • Lupin entered an exclusive agreement with Gan & Lee Pharmaceuticals for bofanglutide, a novel fortnightly GLP-1 receptor agonist.
  • Bofanglutide targets type 2 diabetes and weight management for overweight/obese individuals, offering once-every-two-weeks convenience.
  • Clinical data suggests bofanglutide provides comparable or better weight loss results than existing GLP-1 alternatives.
  • The partnership strengthens Lupin's diabetes portfolio and expands its presence in India's growing obesity market.

Why It Matters: Lupin delays VISUfarma deal but strengthens its diabetes and obesity segments with a new fortnightly drug.

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