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Sourced directly from the authorized manufacturer network to ensure authenticity and quality.
Ready to proceed? Start a request for Cofrogliptin 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:
China
Regulatory Approval:
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Cofrogliptin is a tablet for type 2 diabetes that you take just once every two weeks. It was discovered and developed in China by Haisco Pharmaceutical Group, and is sold there as 倍长平® (Bei Chang Ping). Haisco describes it as the first DPP-4 inhibitor anywhere designed to be taken every two weeks, which works out to 26 doses a year instead of a tablet every day.
China's National Medical Products Administration (NMPA) approved it in June 2024 to improve blood sugar control in adults with type 2 diabetes. The Chinese label allows it to be used:
It is not meant for type 1 diabetes or diabetic ketoacidosis. It is a prescription endocrinology medicine and should be used under the care of a diabetologist or endocrinologist.
After a meal, the gut releases hormones called GLP-1 and GIP that tell the pancreas to release insulin and cut back on glucagon. An enzyme called DPP-4 breaks these hormones down quickly. Cofrogliptin blocks DPP-4, so more of the active hormones stay in the blood and insulin is released only when blood sugar is high. That glucose-dependent action is why the risk of low blood sugar is low. What makes it different is how long it stays in the body: at the 10 mg dose its half-life is about 131.5 hours, and a single dose keeps DPP-4 more than 80% blocked across the full two weeks.
Two phase 3 trials in China supported its approval, each with a 24-week double-blind period followed by a 28-week open extension:
Your doctor will confirm the plan, including what to do if more than one dose is mixed up.
This information is not a treatment plan. For personalized medical advice, consult your doctor and refer to the full prescribing information.
Overall: in the two phase 3 trials, side effects were mostly mild and passed without treatment or stopping the medicine. The most common was a rise in the enzyme lipase on blood tests (4.5% on 10 mg vs 1.9% on placebo), followed by raised amylase (1.3% vs 0.6%), abnormal liver tests (1.9% vs 1.3%), urinary tract infection (1.3% vs 0.6%) and high uric acid (1.0% vs 0%).
Who should not take it: anyone allergic to cofrogliptin or any ingredient of the tablet. It is not recommended in pregnancy or breastfeeding, and its safety in people under 18 has not been established. Long-term heart safety studies have not yet been done.
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.
The tablets can be imported only in the patient's name, by the patient or a government hospital, in line with India's import regulations for unapproved medicines. You will need:
Once we have received and checked a valid prescription and, where needed, an import permit.
No. It is approved only in China. It does not appear in CDSCO's lists of new drugs approved in India, it is not sold in Indian pharmacies, and the US FDA and European Medicines Agency have not approved it either.
Patients can still get it legally through the Named Patient Program (NPP), which allows a medicine not registered in India to be imported for one specific patient on a prescription. Because it is taken only twice a month, a few boxes cover several months of treatment.
It can be made available to patients, doctors, and hospitals across major cities in India, including Gurgaon, Delhi, Bangalore, Mumbai, Navi Mumbai, Thane, Hyderabad, Mysore, Kerala, Chennai, Coimbatore, Madurai, Kolkata, Ahmedabad, Surat, Vadodara, Pune, Nagpur, Nashik, Jaipur, Udaipur, Lucknow, Kanpur, Gorakhpur, Chandigarh, Mohali, Faridabad, Noida, Ghaziabad, Kochi, Trivandrum, Kozhikode, Thrissur, Kannur, Mangalore, Bhubaneswar, Patna, Ranchi, Raipur, Guwahati, Visakhapatnam, Vijayawada, Goa, Jammu, Srinagar, Dehradun, Bhopal, Indore, Ludhiana, Amritsar, and others — and can facilitate delivery to the patient's treating hospital. Orders are confirmed only after receipt of a valid doctor's prescription and an import permit, where applicable.
NamedPatientProgram.com (NPP) sources this medicine through the manufacturer's authorised supply channels in China and arranges supply to patients, doctors, and hospitals under applicable legal provisions. Each box holds one blister of four 5 mg tablets, which is two doses, or four weeks of treatment at the usual 10 mg every two weeks. The tablets are kept sealed, protected from light and below 25°C, so they travel in their original packs under temperature-controlled shipping. All prescriptions are dispensed and checked by registered pharmacists and dispatched from New Delhi, India, after legal requirements are fulfilled.
For the current cost in India and availability, contact NPP via WhatsApp at +91 98104 69557 | Toll-Free: 1800-1200-365 or email info@namedpatientprogram.com.
Patients across India can access this medicine through regulated import pathways, with delivery arranged to the patient or the treating clinic on a valid doctor's prescription.
Diabetes clinics in Delhi see patients from across North India, and being close to our New Delhi dispatch point keeps delivery times short.
Diabetologists in Mumbai can request the medicine for a named patient, and several months of supply can be planned in one order.
Patients in Bangalore can have the tablets delivered home or to their clinic once the prescription has been checked.
A major centre for diabetes care in South India, where the treating doctor can send the prescription and HbA1c report to start the import.
Endocrinologists in Hyderabad can coordinate access for patients who would find a two-weekly tablet easier to stick to.
For Kolkata and the eastern states, deliveries are timed so the next two-weekly dose is never missed.
Patients in Pune can use the same documented import route, with updates shared at each stage.
Gujarat has a large number of people living with type 2 diabetes, and doctors here can request supply for individual patients.
Patients in Jaipur and across Rajasthan can receive the tablets at home or at the treating clinic.
Serves patients from Punjab, Haryana and Himachal Pradesh, with delivery to the patient or the clinic.
We arrange delivery to patients and diabetes clinics across Uttar Pradesh.
Kerala has one of the highest diabetes rates in India, and patients here can receive the medicine in Kochi and nearby cities.
Access can also be coordinated for patients in other Indian cities, subject to a valid prescription and regulatory requirements.
Written By
Nitin GoswamiDeputy Manager – Content & Social Media, Ikris Pharma Network
Sources: NMPA • CDSCO
Last Updated: 19 October 2026
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