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Sourced directly from the authorized manufacturer network to ensure authenticity and quality.
Ready to proceed? Start a request for Xiidra on our secure patient portal to submit your prescription, upload documents and track your approval status.
Supplied with complete CDSCO-approved import and customs documentation, including Form 12A & 12B, CDEC, GST Bill of Entry, Commercial Invoice, and Packing List.
Manufacturer / Innovator:
Bausch + Lomb
Regulatory Approval:
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Over a decade of trusted expertise in Named Patient Access to innovative and life-saving medicines.
100% CDSCO-compliant processes ensuring safe, ethical, and responsible medicine access.
Medicines sourced from authorized manufacturers with full batch traceability.
EU-GDP compliant warehousing for secure, quality-controlled global distribution.
Temperature-controlled logistics ensuring safe, reliable, and timely medicine delivery.
Xiidra (lifitegrast ophthalmic solution) is approved by the FDA for the treatment of the signs and symptoms of dry eye disease (DED) in adults.
Xiidra is a lymphocyte function-associated antigen-1 (LFA-1) antagonist. It blocks the interaction between LFA-1 and intercellular adhesion molecule-1 (ICAM-1), a pathway involved in the inflammatory process underlying dry eye disease, helping to reduce inflammation on the eye's surface.
Xiidra is intended for adults experiencing the signs and symptoms of dry eye disease, offering a prescription treatment option targeting the underlying inflammation rather than only lubricating the eye surface.
The recommended dose of Xiidra is one drop instilled in each eye twice daily, approximately 12 hours apart, using a single-use container per dose per eye.
Xiidra does not carry a formal FDA boxed warning. However, patients and prescribers should be aware of the following important safety information.
Xiidra should not be administered while wearing contact lenses. Lenses should be removed prior to instillation and may be reinserted 15 minutes after administration.
Xiidra is contraindicated in patients with known hypersensitivity to lifitegrast or any other ingredient in the formulation.
The most commonly reported adverse reactions, occurring in 5% to 25% of patients, include instillation-site irritation, altered taste sensation (dysgeusia), and reduced visual acuity.
Step 1 – Search & request your medicine: The patient or treating doctor submits a request with basic details to initiate the access process.
Step 2 – Verification & eligibility review: The team verifies availability and reviews eligibility against regulatory and clinical requirements to ensure a compliant pathway.
Step 3 – Receive quote & delivery timeline: A transparent quotation is shared, covering medicine cost, logistics, and a clear delivery timeline.
Step 4 – Regulatory approval process: Assistance is provided to secure the approvals and documentation required for legal cross-border access.
Step 5 – Temperature-controlled import & handling: The medicine is sourced and transported under strict GDP-compliant conditions to maintain product integrity.
Step 6 – Secure delivery: The medicine is delivered to the patient or treating hospital, with updates provided at each stage.
Note: From request to delivery, every step is designed to ensure your treatment reaches you safely, compliantly, and without unnecessary delays.
Xiidra is manufactured and marketed by Bausch + Lomb. It is sourced through authorized distribution channels for patients seeking named-patient import into India.
Patients typically need a valid prescription from a treating ophthalmologist confirming dry eye disease diagnosis. NPP's regulatory team assists in preparing and verifying the documentation needed for a compliant import.
As an FDA-approved therapy for dry eye disease, Xiidra is sourced through authorized channels and imported under GDP-compliant logistics to preserve product quality throughout transit.
NPP sources Xiidra directly from authorized pharmaceutical distributors to ensure product authenticity and full traceability. Every shipment is handled under Good Distribution Practice (GDP) conditions from origin to the patient's doorstep.
Xiidra should be stored at 20°C to 25°C, with excursions permitted between 15°C and 30°C, and this condition is maintained throughout transit.
Once documentation and regulatory approvals are in place, delivery timelines are communicated transparently at the time of quotation, accounting for import clearance and last-mile logistics to the patient's city.
Patients across India can access Xiidra through NPP's regulated import pathway, with ophthalmology specialists in major cities supporting the treatment process.
Leading hospitals in Mumbai support ophthalmology care coordination and documentation for Xiidra access.
Delhi's major hospitals assist patients with prescription support and documentation for Xiidra.
Bangalore's specialist network offers access coordination for eligible dry eye patients seeking Xiidra.
Chennai-based ophthalmology specialists coordinate Xiidra access alongside comprehensive dry eye care.
Hyderabad's care institutions support patients pursuing Xiidra therapy.
Kolkata's specialist centers help coordinate documentation and treatment access for Xiidra.
Pune-based specialists assist with prescription support and Xiidra treatment planning.
Ahmedabad's specialty hospitals support the import and treatment process for Xiidra.
Kochi's specialist units assist patients with the documentation needed for Xiidra access.
Chandigarh's care centers support Xiidra treatment coordination for patients from North India.
Jaipur's specialists help patients navigate the Xiidra access process.
Lucknow-based centers assist patients pursuing Xiidra therapy.
Bhubaneswar's institutions support access to Xiidra for eligible patients.
Guwahati's specialists help coordinate Xiidra access for patients across the Northeast.
Patients in other cities across India can also access Xiidra through NPP's nationwide coordination network.
Our specialists are here to guide you through every step of the medicine access process.
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