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  • Cipla's Lanreotide...

Cipla's Lanreotide Supply in US Hit After USFDA Observations at Pharmathen Facility

Written By : Parthika Patel Published On 2026-01-15T17:46:27+05:30  |  Updated On 15 Jan 2026 5:46 PM IST
Ciplas Lanreotide Supply in US Hit After USFDA Observations at Pharmathen Facility
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Cipla clarified that re-supply of Lanreotide Injection is expected to resume in the first half of FY 2026-27.

New Delhi: Cipla Limited has recently informed that the supply of Lanreotide Injection in the US market will remain temporarily limited following inspectional observations issued by the United States Food and Drug Administration (USFDA) at the manufacturing facility of Pharmathen International S.A., the drug's manufacturer and exclusive supplier.

The disclosure was made under Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015, through an update dated 14 January 2026.

In its communication, Cipla stated that Pharmathen International S.A., based in Greece, manufactures and exclusively supplies Lanreotide Injection to Cipla USA Inc., a wholly owned subsidiary of Cipla Limited in the United States. The company highlighted that Lanreotide is among Cipla’s top three products in the US market.

Cipla disclosed that the USFDA conducted an inspection at Pharmathen’s Rodopi, Greece manufacturing facility from 10 November 2025 to 21 November 2025. Following the inspection, the USFDA issued nine inspectional observations in Form 483. The redacted version of the Form 483 was made public on 7 January 2026, after which widespread media coverage across mainstream platforms led to material movement in Cipla’s share price.

Also Read: Cipla Emerges as Domestic Contender in Anti-Obesity Market with Yurpeak

Subsequently, after evaluating the situation and holding discussions with Pharmathen, Cipla stated that it was informed through its subsidiary Cipla USA Inc. that production of Lanreotide has been temporarily paused. The pause is aimed at supporting ongoing remediation efforts at the manufacturing site in response to the USFDA observations.

The company further clarified that re-supply of Lanreotide Injection is expected to resume in the first half of FY 2026–27. Until manufacturing operations restart and quality clearances are obtained, the product will remain in limited supply in the market.

Cipla emphasized that it is closely monitoring supply levels and reiterated its commitment to restoring a stable and reliable supply of Lanreotide at the earliest.

Also Read: Cipla Gets CDSCO Panel Nod to Begin Phase III Study of Semaglutide Injection
ciplalanreotide injectionusfda inspectionform 483pharmathen greecepharma news
Parthika Patel
Parthika Patel

    M. Pharm (Pharmaceutics)

    Parthika Patel has completed her Graduated B.Pharm from SSR COLLEGE OF PHARMACY and done M.Pharm in Pharmaceutics. She can be contacted at editorial@medicaldialogues.in. Contact no. 011-43720751

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