You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 31, 2025

Drug Price Trends for VIRAMUNE


✉ Email this page to a colleague

« Back to Dashboard


Drug Price Trends for VIRAMUNE

Best Wholesale Price for VIRAMUNE

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available to any customer under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Unit Dates Price Type
VIRAMUNE XR 400MG TAB Boehringer Ingelheim Pharmaceuticals, Inc. 00597-0123-30 30 606.36 20.21200 EACH 2022-09-15 - 2027-09-14 Big4
VIRAMUNE XR 400MG TAB Boehringer Ingelheim Pharmaceuticals, Inc. 00597-0123-30 30 836.10 27.87000 EACH 2022-09-15 - 2027-09-14 FSS
VIRAMUNE XR 400MG TAB Boehringer Ingelheim Pharmaceuticals, Inc. 00597-0123-30 30 629.02 20.96733 EACH 2023-01-01 - 2027-09-14 Big4
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Unit >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market Analysis and Price Projections for VIRAMUNE (Nevirapine)

Last updated: August 1, 2025


Introduction

VIRAMUNE (Nevirapine) remains a critical component in the global management of HIV/AIDS. As a non-nucleoside reverse transcriptase inhibitor (NNRTI), it has been widely used in antiretroviral therapy (ART) regimens since its approval in 1996. Despite the advent of newer therapies, VIRAMUNE sustains demand due to its established efficacy, availability in low-resource settings, and inclusion in fixed-dose combinations. This analysis examines current market dynamics, competitive landscape, pricing trends, and future price projections for VIRAMUNE, offering strategic insights for stakeholders.


Market Landscape Overview

Global Demand Dynamics

The global HIV/AIDS burden, particularly in low- and middle-income countries (LMICs), sustains demand for VIRAMUNE. According to UNAIDS, approximately 38 million people globally live with HIV, with 25.4 million on ART as of 2022 (UNAIDS, 2022). Viramune remains pivotal in first-line regimens where NNRTIs are preferred, especially in regions with limited access to advanced therapies.

While the overall ART market is sizable, the share of VIRAMUNE specifically is gradually declining with the development of integrase inhibitors like dolutegravir, which offer improved tolerability and resistance profiles. Nonetheless, VIRAMUNE continues to hold importance, particularly in resource-strapped settings due to its affordability and inclusion in generic drug portfolios.

Manufacturers and Market Share

Key manufacturers include Mylan (now part of Viatris), Aurobindo Pharma, and Hetero Labs, producing generic VIRAMUNE formulations. The drug's unpatented status in many markets has led to low-cost production, making it accessible in LMICs via global health programs like the Global Fund and PEPFAR.

In high-income countries, usage has diminished due to safety concerns such as hepatotoxicity and rash. Consequently, the premium for VIRAMUNE in these markets is limited, with most sales concentrated in LMICs via bulk procurement channels.


Market Trends and Drivers

Regulatory and Policy Influences

Recent WHO guidelines favor integrase inhibitors over NNRTIs for first-line ART, which impacts VIRAMUNE’s market share. However, the WHO’s conditional recommendation of generic VIRAMUNE for resource-limited settings sustains its relevance. Regulatory approvals continue to evolve, with some countries updating their treatment protocols away from VIRAMUNE in favor of newer agents.

Clinical Preference Shift

The safety profile of VIRAMUNE is inferior to newer drugs, leading to decreased initiation in new patients in high-income settings. Nevertheless, its low cost and proven efficacy in diverse populations uphold its presence in large-scale treatment programs.

Supply Chain and Generic Availability

Global efforts to expand access to affordable ART ensure sustained supply of VIRAMUNE generics. Patent expirations in several jurisdictions facilitate further proliferation of low-cost formulations, maintaining competitive pressure but stabilizing prices.


Price Trends and Historical Data

Current Pricing Landscape

VIRAMUNE's pricing varies significantly across regions:

  • High-income markets: Cost per unit ranges from $0.30 to $0.60 in branded formulations, but actual usage is minimal.
  • LMICs and procurement programs: Generics are available at approximate prices of $0.05 to $0.10 per dose (per 200 mg tablet). Bulk purchasing and international procurement contribute to these low prices.

Pricing Factors

Pricing is driven by:

  • Production costs in generic manufacturing hubs (India, China).
  • Negotiated procurement prices via donor-funded programs.
  • Regulatory environment.
  • Competition among generic producers.

Recent Pricing Trends

Over the past five years, prices for VIRAMUNE generics have decreased by approximately 30-50%, reflecting increased competition and scale economies. The transition towards fixed-dose combinations (FDCs) incorporating VIRAMUNE has affected single-agent prices but boosted overall accessibility.


Future Price Projections (2023–2030)

Projection Methodology

Price projections consider:

  • Patent and regulatory status.
  • Market penetration of newer agents.
  • Manufacturing capacity and competition.
  • Policy shifts in global and national treatment guidelines.
  • Economic factors affecting production costs.

Near-term Outlook (2023–2025)

In the short term, VIRAMUNE prices are expected to stabilize or decline slightly, driven by:

  • Continued generic competition in LMIC markets.
  • Consolidation among generic manufacturers.
  • Donor price negotiations sustained by global health initiatives.

Estimated price range:

  • Per 200 mg tablet: $0.04 to $0.08 in LMICs.
  • Per course (per patient/month): ~$1.20 to $2.40.

Mid- to Long-term Outlook (2026–2030)

Global health policies favor newer, safer, and more tolerable drugs, potentially leading to:

  • Further decline in VIRAMUNE demand in high-income and some middle-income countries.
  • Continued low-cost production in LMICs, maintaining prices at or below current levels.
  • Displacement by integrase inhibitors, though VIRAMUNE will persist in supply chains serving low-resource markets.

Projected price trajectory:

  • Minimal fluctuation; prices likely to hover around $0.03–$0.07 per tablet due to sustained competition.

Impact of Technological and Policy Changes

While advancements in ART continue to favor newer agents, VIRAMUNE’s low-cost generics are expected to retain a foothold in specific markets, particularly where cost is a primary determinant. Anticipated policies promoting affordability may reinforce stable or declining prices.


Market Opportunities and Challenges

Opportunities:

  • Expansion in LMICs with large treatment gaps.
  • Inclusion in commodity-based procurement mechanisms.
  • Strategic partnerships to improve access.

Challenges:

  • Competition from newer agents with superior safety profiles.
  • Evolving international guidelines reducing first-line use.
  • Potential supply disruptions due to manufacturing capacity constraints.

Key Takeaways

  • Stable Demand in LMICs: VIRAMUNE remains essential in resource-limited settings owing to its affordability and established efficacy.
  • Declining Use in High-Income Markets: Safety concerns and newer medications reduce demand, limiting price growth potential.
  • Price Trends: Generics continue to drive down prices, with expected stabilization at low-cost levels (around $0.04–$0.07 per tablet).
  • Future Outlook: Marginal price reductions are anticipated due to sustained generic competition, with the drug maintaining a niche role primarily in LMICs.
  • Strategic Focus: Stakeholders should prioritize supply chain resilience and cost-effectiveness to capitalize on ongoing demand in accessible markets, while monitoring regulatory shifts influencing future market dynamics.

FAQs

1. Will the price of VIRAMUNE increase due to growing demand in developing countries?
Unlikely. The demand remains stable primarily in low-resource settings, where generic competition keeps prices low. Increased demand does not significantly influence prices in these markets.

2. How will newer ART drugs impact VIRAMUNE's market share?
The advent of integrase inhibitors like dolutegravir is reducing VIRAMUNE's use in first-line regimens, especially in high-income countries, potentially limiting its overall market growth.

3. Is there potential for price increases if VIRAMUNE faces supply shortages?
While shortages could temporarily raise prices, the high level of generic manufacturing competition mitigates this risk. Supply agreements with large procurement agencies further stabilize prices.

4. What role will global health initiatives play in VIRAMUNE pricing?
Organizations like the Global Fund and PEPFAR negotiate procurement prices, contributing to sustained low costs and preventing price hikes driven by market scarcity.

5. Are there regulatory barriers that could influence future prices?
Regulatory changes favoring newer drugs or restrictions on older formulations may reduce demand, indirectly affecting prices by decreasing market size and competition.


References

  1. UNAIDS. Global HIV & AIDS statistics — 2022 fact sheet. (2022).
  2. World Health Organization. Consolidated guidelines on HIV prevention, testing, treatment, service delivery, and monitoring — 2021 update.
  3. MarketResearch.com. HIV/AIDS antiretroviral drugs market report — 2022.
  4. IMS Health. Global ART drug price trends — 2018-2022.
  5. Global Fund. Procurement data and partner country reports — 2023.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.