FDA cancels drug sale licences of Cipla Pharma & Life Sciences' Pune Carry and Forwarding unit
The regulator seized stock worth ₹11.19 lakh after finding misbranded packaging, storage lapses and recall failures at the company’s Pune unit.
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7 Articles
The Maharashtra FDA has revoked the drug sales license of Cipla's Pune C&F Center. The administration took this action after an investigation into the Reactin Plus tablets revealed irregularities and violations. The company has also been directed to withdraw the drugs from the market.
FDA cancels Cipla Pune unit's licence over Reactin Plus storage, record lapses
The action was taken after an inspection of the company's Wadki facility found discrepancies between physical stock and computerised records, lapses in stock management and inadequate storage arrangements.
Maharashtra FDA Cancels Cipla Unit’s Drug Sales Licence Over Storage, Regulatory Violations | 📰 LatestLY
The Maharashtra Food and Drug Administration (FDA) has cancelled the drug sales licences of Cipla Pharma & Life Sciences’ Carrying and Forwarding (C&F) unit in Pune, citing storage deficiencies and regulatory non-compliance. 📰 Maharashtra FDA Cancels Cipla Unit’s Drug Sales Licence Over Storage, Regulatory Violations.
Misbranding, storage lapses: FDA cancels Cipla Pune unit’s drug licence over Reactin Plus violations
The Maharashtra Food and Drug Administration has revoked Cipla's licenses to sell Reactin Plus Tablets due to serious violations in packaging and storage practices. Medicines were improperly stored on the floor, and the handling of expired products was inadequate. Cipla also failed to comply with the necessary recall protocols for misbranded drugs. The authorities emphasized that stringent measures will be implemented to ensure adherence to drug…
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