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Drug pricing & your rights

Cancer Drug Price Control in India — Checking Your NPPA Ceiling Before You Pay

India's government caps the price of hundreds of cancer medicines under law. If your drug is on the list, no pharmacy can legally charge above the published ceiling — and you can look up that ceiling yourself before you pay.

  • Prices are legally capped — NPPA sets ceiling prices for medicines on the National List of Essential Medicines under the Drug Price Control Order.
  • The list is public — Anyone can search the NPPA database to find the ceiling price for a listed drug before visiting a pharmacy.
  • Brand and generic share the same ceiling — If a drug is under price control, that ceiling applies whether you buy the originator brand or a generic version.
  • The price gap between versions can be very large — Originator brands and generics of the same molecule can differ substantially in cost — the ceiling tells you what either must not exceed.

Medically reviewed by Dr. C. Raghavendra Reddy, Medical Oncologist, MBBS (Gold Medal) · DNB · DM (Medical Oncology, Gold Medal) · Last reviewed September 2026

Prescription-only medicine. Cancer medicines are prescription-only drugs, given under the supervision of a specialist oncologist. Nothing on this page is a substitute for a medical consultation, and no cancer treatment should be started, changed, or stopped based on anything you read online. Nothing on this page is a recommendation to use this medicine. It is not suitable for most patients — see "Who this is not for" below.

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Yes — India's NPPA sets ceiling prices for hundreds of cancer medicines under the Drug Price Control Order. If a drug is on this list, no pharmacy can legally charge above the published ceiling. You can check the ceiling for any listed medicine on the NPPA website before you pay.

What is the difference between a branded, a generic, and a biosimilar cancer medicine?

FeatureOriginator / brand-nameGeneric (small molecule)Biosimilar (biological)
What it isThe original compound, developed and first approved by its manufacturerThe same active molecule at the same dose, proven to behave identically in the bodyA biological medicine — made from living cells — shown to be highly similar to the originator biologic
Approval route in IndiaFull new drug application submitted to CDSCOAbbreviated route proving bioequivalence to the originatorDedicated similarity pathway — more demanding than for small-molecule generics
Quality standardCDSCO Good Manufacturing PracticeCDSCO Good Manufacturing PracticeCDSCO Good Manufacturing Practice
NPPA ceiling applies?Yes, if listed under NLEM or DPCO ScheduleYes, if listed under NLEM or DPCO ScheduleYes, if included in NLEM — not all biosimilars currently qualify
Price relative to originatorReference — the price everything else is compared againstCan be substantially lower; the gap varies widely by drug and marketGenerally lower than the originator biologic; exact gap varies by molecule
Prescription required?Yes — Schedule H or H1 depending on the drugYes — Schedule H or H1 depending on the drugYes — Schedule H or H1 depending on the drug

How do you check if your cancer drug has a ceiling price?

The NPPA publishes ceiling prices in a publicly searchable database at nppaindia.nic.in. Search by the salt name — the active molecule — rather than the brand name. Most cancer drugs are listed by their international non-proprietary name, not by the brand printed on the box.

The ceiling price in the database is the maximum the manufacturer is permitted to charge before trade margins are added. The MRP printed on the physical pack reflects this figure plus retailer margins and applicable taxes. What you pay at the counter must not exceed the MRP on the pack.

If a drug does not appear in the NPPA database, it may not currently be under price control. The NLEM is revised periodically, so a drug not listed today may be added at the next revision. Your hospital pharmacist can tell you whether a specific medicine currently carries a government ceiling.

Who should not have chemotherapy?

Chemotherapy is not appropriate for everyone, and the decision is made by your oncologist based on the individual clinical picture, not on any general list.

People who are generally not candidates for cytotoxic chemotherapy include:

  • Those with very poor performance status, where the body cannot safely tolerate the treatment
  • People with severely reduced kidney or liver function, as most chemotherapy agents are cleared through these organs
  • Patients with active, uncontrolled infection, as chemotherapy further suppresses the immune system
  • Those in the first trimester of pregnancy, where most cytotoxic agents carry a high risk of harm to the foetus
  • People whose cancer type or molecular profile does not respond to chemotherapy, where targeted therapy or another approach is more appropriate

Eligibility is decided by your oncologist on the basis of your diagnosis, test results, and general health. No list replaces that assessment.

What do NPPA, DPCO, NLEM and these other terms mean?

NPPA
National Pharmaceutical Pricing Authority — the government body that sets, monitors, and enforces ceiling prices for medicines in India.
DPCO 2013
Drug Price Control Order 2013 — the legal instrument that gives NPPA authority to fix prices for scheduled medicines without requiring the manufacturer's agreement.
NLEM
National List of Essential Medicines — the government's list of drugs considered essential to public health. Most cancer drugs on this list carry an NPPA ceiling price.
Ceiling price
The maximum price NPPA permits a manufacturer to charge for a scheduled drug. The retail price you pay is derived from this figure, after adding allowed trade margins and taxes.
MRP
Maximum Retail Price — the highest price any retailer, including a hospital pharmacy, can legally charge. It is printed on the pack and must not be exceeded.
Bioequivalence
Proof, required by CDSCO, that a generic medicine reaches the same concentration in the bloodstream in the same timeframe as the originator. It is the basis for treating a generic as therapeutically equivalent.
Biosimilar
A biological medicine — derived from living cells — approved as highly similar, but not structurally identical, to an already-approved originator biologic. Biosimilars follow a separate regulatory pathway from small-molecule generics.

Did you know?

Under the Drug Price Control Order 2013, the Indian government can fix the maximum price of any medicine it classifies as essential — without waiting for the manufacturer to agree.

This authority has been used specifically for cancer medicines. When NPPA issues a ceiling price notification, it is published in the Official Gazette and takes effect immediately.

Source: Drug Price Control Order 2013, Ministry of Chemicals and Fertilizers

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Common questions

Frequently asked questions

Can a pharmacy legally charge more than the ceiling price?

No. If a drug is listed under the DPCO, the MRP printed on the pack must not exceed the NPPA ceiling, after allowed trade margins and taxes are added. Charging above the printed MRP is a violation of the DPCO, whether the pharmacy is a standalone shop or part of a hospital. If you suspect overcharging, compare what you were charged against the MRP on the physical packaging — that figure is your legal reference, not the receipt alone.

What should I do if I think I have been overcharged for a cancer medicine?

Start by checking the MRP printed on the pack against what you paid. If the pack MRP is lower than what you were charged, keep the receipt and the packaging together — you will need both. You can file a complaint with your state drug controller's office, or raise the matter through the National Consumer Disputes Redressal Commission. For a scheduled medicine under DPCO, overcharging is a punishable offence and both bodies have authority to act.

Does the price ceiling apply inside hospitals, or only at retail pharmacies?

The ceiling operates at the manufacturer level, and the MRP printed on the pack applies to all retail sales — including hospital pharmacies. No pharmacy, hospital-based or otherwise, can charge above the pack MRP for a scheduled medicine. Hospitals may separately charge a service or dispensing fee in some states, but they cannot charge above the pack MRP for the drug itself. If the pack MRP is being exceeded, it is a violation in any setting.

Is the generic version of a cancer drug as safe as the brand-name version?

A generic approved by CDSCO has demonstrated bioequivalence to the originator — the same active molecule, absorbed in the same way, at the same rate. The manufacturing standard required is the same. The price difference does not reflect a difference in the active substance. Your oncologist or treating pharmacist is the right person to confirm whether a specific generic is appropriate for your regimen, since formulation details can sometimes matter in oncology settings.

How do I search the NPPA website for my drug's ceiling price?

Go to nppaindia.nic.in and use the drug price search. Search by the salt name — the generic name of the active molecule — rather than the brand name. Most cancer drugs appear under their international non-proprietary name. The ceiling price shown is the manufacturer-level maximum before margins and taxes are added. If your drug does not appear, it may not currently be under price control — your hospital pharmacist can confirm.

Are biosimilar cancer drugs covered by price control in India?

Biosimilars included in the National List of Essential Medicines are subject to NPPA ceiling pricing in the same way as listed small-molecule drugs. Not all biosimilar cancer medicines are currently on the NLEM, so not all carry a government-set ceiling. The NLEM is revised periodically, and a biosimilar not currently listed may be added at the next revision. Your hospital pharmacist can tell you whether a specific biosimilar has a price ceiling, and the NPPA database at nppaindia.nic.in is the primary reference.

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