
Lupin Limited has expanded its US injectable portfolio with the launch of Sugammadex Injection following approval from the United States Food and Drug Administration (US FDA), as per the exchange filings.
The product has been introduced in 200 mg/2 mL (100 mg/mL) and 500 mg/5 mL (100 mg/mL) strengths, both available as Single-Dose Vials.
Lupin's newly launched injection is bioequivalent to Bridion Injection from Merck, Sharp & Dohme LLC (Merck).
The company received approval for its Abbreviated New Drug Application (ANDA) before commercially introducing the product in the United States.
Sugammadex Injection is used for the reversal of neuromuscular blockade caused by rocuronium bromide and vecuronium bromide.
Its approved use covers adults and paediatric patients aged two years and above undergoing surgery.
Headquartered in Mumbai, Lupin distributes its products across more than 100 markets. Its portfolio spans branded and generic formulations, complex generics, biotechnology products and active pharmaceutical ingredients.
The company has established positions in India and the US across respiratory, cardiovascular, anti-diabetic, anti-infective, gastrointestinal, central nervous system and women's health therapies.
Lupin operates 15 manufacturing sites and seven research centres globally, supported by a workforce of more than 26,000 professionals.
Its subsidiaries include Lupin Diagnostics, Lupin Digital Health and Lupin Manufacturing Solutions.
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As of 31 July 2026, at 2:56 PM, Lupin Ltd share price was trading at ₹2,411.70 per share, reflecting a decline of 0.39% from the previous trading session.
The US launch adds Sugammadex Injection to Lupin's product portfolio in two single-dose vial strengths. The product is intended to reverse specific neuromuscular blockades in surgical patients aged two years and above.
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Published on: Jul 31, 2026, 3:45 PM IST

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