NPPA fixes retail prices of 39 drug formulations, raises anti-rabies immunoglobulin rate
Synopsis
Key Takeaways
The National Pharmaceutical Pricing Authority (NPPA) has raised the retail price of anti-rabies immunoglobulin and fixed the retail prices of 39 drug formulations spanning treatments for hypertension, diabetes, HIV, heart disease, and eye infections, under its latest regulatory exercise pursuant to the Drugs (Prices Control) Order (DPCO). The decisions were formalised through a gazette notification issued following the authority's 148th meeting.
Anti-Rabies Immunoglobulin Price Revision
The retail price of anti-rabies immunoglobulin has been revised upward to ₹119.48 per millilitre (ml) from the earlier ₹112.19 per ml, reflecting an increase of 6.49 per cent. The revision is in line with the NPPA's March 2025 decision to permit a 0.64956 per cent annual price increase for medicines on the National List of Essential Medicines (NLEM), calibrated against changes in the Wholesale Price Index (WPI).
Key Drug Formulations Priced
Among the 39 formulations assigned retail prices, a fixed-dose combination (FDC) of amlodipine, bisoprolol, and telmisartan tablets — prescribed for the management of hypertension — has been priced at ₹14.74 per tablet. A cardiology formulation combining clopidogrel, aspirin, and atorvastatin capsules, used to reduce the risk of heart attacks and strokes, has been assigned a ceiling of ₹6.37 per capsule.
In ophthalmology, the NPPA fixed the retail price of nepafenac and moxifloxacin ophthalmic solution — indicated for eye infections — at ₹68.64 per ml. The authority noted that any manufacturer or marketing company found charging above the notified retail rates would be required to deposit the overcharged amount along with applicable interest under the relevant DPCO provisions.
Pneubevax 14 Exempted from Price Control
In a separate decision, the NPPA granted a five-year exemption from price control to Pneubevax 14, described as India's first 14-valent Pneumococcal Polysaccharide Conjugate Vaccine, developed and manufactured by Hyderabad-based Biological E. The vaccine qualified for exemption under Paragraphs 32(i) and 32(ii) of the DPCO, 2013, as it is covered by a granted patent and meets the criteria applicable to new drugs developed through indigenous research and development.
Under these provisions, a patented new drug developed domestically and not manufactured elsewhere is exempt from the price control order for five years from the date commercial production begins in India. The NPPA has directed Biological E to submit details of the dates of commercial production and commercial marketing of the vaccine, along with the price to retailer (PTR) and the maximum retail price (MRP) set by the company.
Regulatory Rationale
The NPPA characterised the exercise as a routine regulatory function aimed at implementing DPCO provisions, regulating both controlled and decontrolled medicines, and ensuring that essential drugs remain financially accessible to patients. This comes amid sustained pressure on public health budgets and recurring concerns from patient groups about the affordability of combination therapies for chronic conditions such as hypertension and diabetes. The pricing decisions are expected to provide some cost certainty for pharmacies and hospitals procuring these formulations.