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Maximum price





Here you will find information about price applications and reevaluation of prices.

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    ​​​​​​​​​Determination of maximum price

    All registered, prescription-only medicines (POM) for humans must have a maximum price, set by the Norwegian Medical Products Agency (NoMA), before they can be marketed in Norway. The market authorization-holder must apply for a maximum price.

    Price application/information form. 

    The maximum pharmacy purchase price (PPP) and the pharmacy mark-up is determined by NOMA. The maximum PPP and mark-up add up to the maximum pharmacy retail price (PRP).

    The maximum PPP is set as the mean of the three lowest market prices of the product in a selection of European countries. The price comparison group includes Sweden, Finland, Denmark, Germany, Great Britain, The Netherlands, Austria, Belgium and Ireland. For more information regarding price setting see the following link:

    Guidelines for price setting in Norway

    The rules for setting, controlling and adjusting prices on medicinal products are described in regulation «Forskrift om legemidler» (chapter 12, in Norwegian). The Norwegian Medical Products Agency (NOMA) provides the following guidelines for setting maximum prices. 

    NOMA will normally follow the main rules when setting prices for medicines. However, in some cases it will be necessary to deviate from these guidelines. NOMA will handle individual cases on a non-discriminatory basis. 

    International price comparisons

    According to forskrift om legemidler § 12-2, prices in other countries in the European Economic Area serve as the main basis for price settlements. The price of a prescription-only medication in Norway is set as the mean of the three lowest market prices of the product in a selection of countries. 

    The reference countries that are included in the price comparison are: Sweden, Finland, Denmark, Germany, UK, Netherlands, Austria, Belgium and Ireland. In a situation where market prices exist in three or fewer of these countries, the price will be set as the average price of the existing prices.

    We request prices valid at the time of reporting.

    NOMA will set prices according to its own estimates if price details which are considered necessary for pricing the medicinal product in Norway have not been received from the Marketing Authorisation Holder on request and within specified deadlines.

    Market price as basis

    NOMA’s price settlement is done on the basis of the actual market price for each of the countries in the price comparison group. The market price is defined as the price the greatest part of the market pays for the product.

    Price is set as PPP

    The price set by NOMA is the maximum sales price to the pharmacy (PPP – pharmacy purchasing price, in Norwegian called AIP, apotekenes innkjøpspris)). The product may freely be sold at a lower price than max PPP.

    Exchange rates

    Price comparisons are based on the price in local currency, converted to NOK. The mean exchange rate of the last six months, as presented by the Central Bank of Norway (, is used to convert prices to NOK.

    Reevaluation of the price in Norway

    According to forskrift om legemidler § 12-5 the Marketing Authorization Holder or the NOMA may suggest a reevaluation of prices if this is justified by changes of circumstances or new information.

    Prices are not normally reevaluated more than once per year. The prices of newly-launched products are exempt from this rule. In the two year period after a launch, NOMA may request information about new prices half-yearly from the MAH with regard to pricing in Norway.

    Withdrawal of a product from one of the reference countries may affect the price in Norway. Documentation must be presented to show that a product has in fact been withdrawn from the market if this is to give cause for price changes.

    Comparable pack-sizes

    Pack sizes are not always directly comparable. Price comparisons with other countries are therefore done on the basis of units. This means that price per tablet, price per dose etc. is compared.

    When setting the price, differentiation is normally made between the price per unit in large and small packages. A package containing 30 or fewer units is normally defined as small. Packages containing more than 30 units are defined as large.
    For some medicinal products and pharmaceutical formulations there are exemptions from the general rule. Those are;

    • Medicinal products for treatment of asthmatic conditions: a package containing 120 or fewer doses is normally defined as small and a package containing more than 120 doses is defined as large.
    • Some products which are used in the treatment of acute migraine attacks and medicines for erectile dysfunction. Packages are defined as small if they contain 5 or fewer tablets and large if they contain more than 5 tablets
       Injectables/injections: Distinction is made as follows: 0 – 5 ml, 6 - 99 ml and 100 ml or more. Vials, bottles, ampoules etc. are compared per unit (with the same amount/number of ml) if each vial, bottle, ampoule etc contains up to and including 5 ml,
    • Injectables/infusions: division is made as follows: 0 – 5 ml, 6 ml - 1000 ml.
      Price per unit in large and small packages

    In some cases, when comparing prices from different countries, the price per tablet in a small package may be lower than the price per tablet in a large package. In such cases, the price per tablet in the large package is set equal to the price per tablet in the small package. If the price per tablet is higher in a small package than in a large package the price difference is accepted provided that the difference is not considered unreasonable.

    Price ratios between different strengths

    When setting the price, NOMA will aim at a reasonable price ratio between different strengths of a given product. This also applies when the products have different names, while they actually are the same.

    Comparable medicines

    When setting the price of a medicinal product in Norway, comparisons will mainly be made with the price of the same product in the reference countries. If medicinal products are marketed under different product names in different reference countries, they will still be compared in the pricing process. Different varieties of the same product may also be taken into consideration when comparing prices. Ex. tablets, capsules, melting tablets, soluble tablets and effervescent tablets will be considered as varieties of the same pharmaceutical. NOMA will only set a higher 
    price for other varieties of the same medicine on exception.

    Parallel import

    The prices of medicinal products which are parallel imported to Norway are limited upwards to the maximum price of the directly imported medicinal product.


    For ATC codes with no packages in the stepped price model, generic medicinal products will get the lowest maximum PPP of medicines within the same ATC code, regardless of whether their marketing authorization is based on biosimilar, well-established use or full dossier applications.

    In ATC codes with packages in the stepped price model, generics may get the same maximum price as the full dossier product.

    There is no need to report prices from reference countries for generics.

    Biosimilars and well-established use

    In ATC codes with no packages in the stepped price model, medicinal products with marketing authorisation (MA) based on a similar biological application or a well-established use application get the lowest maximum PPP of the following:

    • maximum PPP as calculated by price comparison with the reference countries
    • lowest maximum PPP of medicinal products within the same ATC code, regardless of whether the MA-application is for similar biological, well-established use or full dossier.

    Price applications for biosimilars and well-established use medicines shall therefore hold prices from the nine reference countries in cases where there are no packages in the stepped price model in the ATC code.

    For ATC codes with packages in the stepped price model, biosimilars and well-established use medicines may get the same maximum price as the full dossier product. For these products there is no need to report prices from reference countries.

    Exceptions to the general rules

    In some situations, it may be appropriate to set a higher maximum PPP than the general rules indicate.

    Two conditions must apply to justify deviation from the main rules:

    1. There is a major risk that the medicine will not be available in the market if the calculated maximum price is implemented.
    2. The absence of the medicine from the market could have negative consequences for the availability of cost-effective medicines.

    If these conditions apply, NOMA will consider setting a higher price based on discretionary judgment. The following circumstances will be considered:

    • Documented production costs
    • Special circumstances regarding the basis for price-calculation.

    The same principles apply in cases with very low stepped prices.

    Time limit

    NOMA shall set new prices within 90 days after receiving a price application, cf. forskrift om legemider § 12-16

    In the 1st quarter of 2024, 51​% of the price applications were processed within 50 days. In the preceeding quarter the result was 29%. The average processing time in the 1sth quarter of 2024 was 47 days.​​

    Exchange rate

    Prices from the reference countries are submitted in local currency. To convert prices into Norwegian kroner (NOK), NOMA uses the mean exchange rate of the last six months, as presented by the Central Bank of Norway (

    List of products with maximum prices

    The list shows the maximum PPP (exclusive VAT) and the maximum PRP (inclusive VAT).Please note that actual prices may be lower than maximum prices stated.

    The Health Enterprises (hospitals) usually obtain discounts in their purchases.

    The Directorate of Health has entered into managed-e​ntry ​agreements (MEA) with MA-holders for Repatha, Praluent, Aimovig, Ajovy and Emgality. The MEAs include an agreed and confidential discount for medicines reimbursed by the National Insurance Scheme.

    There is no price regulation for over the counter medicines, products without marketing authorization and veterinary medicines.

    Reevaluation of maximum prices

    The marketing authorization holder and NOMA may initiate a reevaluation of the maximum prices. However, adjustments should normally not occur more frequently than once per year. NoMA reevaluates the maximum price for the active ingredients with the highest turnover. The purpose is to ensure that the maximum prices reflect the developments in European prices.​​

    Bindings on the maximum price which are due to NOMA’s prior decisions about reimbursement by the National Insurance Scheme, cease when medicines aretransferred to reimbursement on H-prescription.

    When reimbursement of a stepped price medicine is transferred from the National Insurance Scheme to H-prescription, the stepped price ceases from the same date as agreed price between The Norwegian Hospital Procurement Trust (Sykehusinnkjøp HF) and the suppliers enters into force.        

    In the end of August/early September each year, NoMA p​ublishes the reevaluation order for the upcoming year. NOMA determines the active ingredients that will be reconsidered, and in what order.

    Timetable for reevalution of prices 2022
    Timetable for reevalution of prices 2023

    Timetable for reevaluation of prices 2024​

    List of products that NOMA will ask for in ​the following month.​​

    Contact us

    Unit for price regulation and market analysis

    22 89 77 00