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National Pharmaceutical Pricing Authority

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Namestring
National Pharmaceutical Pricing Authority
Legal namestring
National Pharmaceutical Pricing Authority
Websiteurl
nppa.gov.in
Company typeenum
Private
Founded yearint
1997
Descriptiontext

National Pharmaceutical Pricing Authority (NPPA) is a statutory regulatory authority constituted by Government of India Resolution on 29 August 1997 and attached to the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers. It functions as the sole independent regulator for pharmaceutical pricing in India under the Essential Commodities Act, 1955 and the Drugs (Price Control) Order, 2013, fixing and revising ceiling prices for scheduled formulations and retail prices for new drugs.

NPPA operates three core digital and physical platforms: the Integrated Pharmaceutical Database Management System (IPDMS 2.0), which captures production, import, export, market share, and profitability data from manufacturers across bulk drugs and formulations; the Pharma Sahi Daam App/Portal, a consumer-facing tool for verifying ceiling prices and filing overcharging grievances; and the Price Monitoring and Research Units (PMRUs), field offices in 32 State/UTs that execute monitoring, public awareness, and enforcement. Ceiling prices have been issued for 928 scheduled formulations and retail prices for approximately 3,111 new drugs. Price regulation has been extended into medical devices (coronary stents, knee implants, anti-rabies immunoglobulin, IV fluids) and, in public-interest interventions under Para 19 of DPCO 2013, into 106 anti-diabetic and cardiovascular drugs and 42 anti-cancer drugs (the latter generating reported savings of up to 90%, or Rs. 984 crores per annum, across 526 brands).

NPPA does not generate commercial revenue. It is wholly funded through Government of India budget allocations and does not charge for regulatory services. Its "customers" in the functional sense are Indian citizens and patients (beneficiaries of price control), pharmaceutical manufacturers and distributors (regulated entities filing Form IV and pricing submissions through IPDMS 2.0), State Drug Controllers (enforcement network), and government health schemes such as Ayushman Bharat. Leadership comprises a Chairman, Member Secretary, and authority members drawn from CDSCO, the Department of Expenditure (Chief Adviser - Cost), and the Department of Economic Affairs (Economic Adviser).

Short descriptiontext

National Pharmaceutical Pricing Authority is the sole statutory regulator of pharmaceutical and medical device pricing in India, operating under the Department of Pharmaceuticals to fix ceiling prices, monitor compliance, and serve citizens, manufacturers, and government health schemes via IPDMS 2.0 and a 32-State PMRU network.

Operating statusenum
Operating
Ownership categoryenum
akta.pro rankint
HeadquartersNew Delhi, India
HQ citystring
New Delhi
HQ countrystring
India
HQ regionstring
Asia
Markets served

Serves global market

Keyword5 values
drug price regulation, pharmaceutical pricing, ceiling price fixation, medicine affordability, pharmaceutical policy
Industry2 codes
1Drug Regulators (Human Pharmaceuticals)
CodeHLAJADAAPrimaryYes
2Government Pricing & Compliance (Medicare/Medicaid/340B/AMP/Best Price)
CodeHLAIAKAEPrimaryNo
Product category
Pharmaceutical Price Regulation
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Technology or R&D, Infrastructure, Others
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 3 records shown
1Pharma Sahi Daam
Description

A platform/app for information on medicine prices and registering public grievances.

nppa.gov.in
+2 more records
Core offering1 text field

National Pharmaceutical Pricing Authority (NPPA) is the statutory regulator for pharmaceutical pricing in India, constituted in 1997 under the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers. It fixes and revises ceiling prices for drugs notified under Schedule-I of the Drugs (Price Control) Order (DPCO) 2013, provides retail prices for new drugs, regulates prices of medical devices (coronary stents, knee implants), and operates digital platforms (IPDMS 2.0 and Pharma Sahi Daam) plus a 32-state PMRU network to monitor compliance, prevent overcharging, and ensure affordable access to essential medicines.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

NPPA operates as a regulatory body rather than a commercial product company. Its primary digital offerings include the Pharma Sahi Daam App/Portal for consumer price verification and grievance registration, the Integrated Public Database Management System (IPDMS) 2.0 for pharmaceutical data management, and a network of Price Monitoring and Research Units (PMRUs) across 32 states. These work together as part of the CAPPMS framework to regulate and monitor drug prices, ensure availability of affordable medicines, and handle public complaints.

Product and service4 records
1Pharma Sahi Daam App/Portal
CategoryPublic Information Platform
Description

Mobile app and web portal that enables consumers to verify ceiling prices of scheduled medicines and register public grievances about overcharging by pharmaceutical companies or retailers. Built for Indian citizens seeking price transparency for essential and life-saving medicines.

2Integrated Pharmaceutical Database Management System (IPDMS) 2.0
CategoryRegulatory Data Management System
Description

Comprehensive digital platform for managing, regulating, and monitoring prices of pharmaceutical products and medical devices. Enables online information collection from pharmaceutical manufacturers and serves as a significant step towards enhancing transparency, efficiency, and accountability in the pharmaceutical and medical devices sector. Used by pharmaceutical manufacturers for compliance submissions.

3Price Monitoring and Research Units (PMRUs)
CategoryField Monitoring Network
Description

State/UT-level field units for strengthening monitoring, public awareness, and enforcement of drug pricing regulations across India. Currently operational in 32 State/UTs as NPPA's decentralized enforcement and outreach arm.

4CAPPMS (Consumer Awareness, Price Monitoring and Public Grievance System)
CategoryConsumer Awareness and Grievance System
Description

Integrated framework for consumer awareness on drug pricing, monitoring of pharmaceutical prices, and handling of public grievances. Operates through PMRUs across states and integrates with the Pharma Sahi Daam portal and IPDMS 2.0.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierCoreTypeOthers
Description

NPPA is an attached office of the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers. It implements the National Pharmaceutical Pricing Policy, 2012 and the Drugs (Price Control) Orders issued by DoP. Powers are delegated to NPPA for fixing and revising drug prices as per DPCO provisions.

2Drug Controller General of India (CDSCO), Ministry of Health and Family Welfare
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Collaboration with CDSCO for integrated data collection, regulation, and improved services. Dr. Rajeev Singh Raghuvanshi serves as Drugs Controller General of India and is a member of NPPA Authority.

nppa.gov.in
3Price Monitoring and Research Units (PMRUs) in 32 State/UTs
Strategic tierCoreTypeOthers
Description

PMRUs established at State/UT levels for strengthening, monitoring and public awareness on drug pricing. NPPA is expanding outside Delhi through these units.

nppa.gov.in
Strategic tierMinorTypeStrategic or Co-development Partner
Description

NPPA seeks to synergize with NIPERs for integrated data collection and undertake concurrent research and studies to enable credible contribution to policy development.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

NPPA collaborates with State Drug Controllers for integrated data collection, regulation, and improved services to the people. State Drug Controllers are listed as related entities on NPPA website.

6Department of Expenditure, Ministry of Finance
Strategic tierCoreTypeOthers
Description

Anand Kumar Pal, Chief Adviser (ICoAS) from the Office of Chief Adviser (Cost), Department of Expenditure, serves as a member of NPPA Authority.

nppa.gov.in
Strategic tierCoreTypeOthers
Description

Dr. Rose Mary K. Abraham, Economic Adviser from Department of Economic Affairs, serves as a member of NPPA Authority.

Strategic tierMinorTypeOthers
Description

Pharmaceutical manufacturers operating in India who submit pricing data through IPDMS 2.0 and comply with DPCO regulations. Estimated over 60,000 medicines sold by over 2,30,000 retail chemists in trade channel.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeOthers
Description

Global pharmaceutical data, analytics, and consulting provider. Comparable on the data-infrastructure layer NPPA relies on (IPDMS 2.0), but as an enabling technology vendor rather than a regulatory peer.

TypeBroad incumbent
Description

The US federal regulator for drugs, biologics, medical devices, and food. A broader incumbent in the same regulatory space; FDA also engages in pricing-adjacent work through Centers for Medicare & Medicaid Services, though its core mandate is safety and efficacy rather than price.

TypeBroad incumbent
Description

Australia's regulator for therapeutic goods including medicines and medical devices. Broader incumbent in the same regulatory family; pricing happens separately via the Pharmaceutical Benefits Scheme, so TGA is most comparable on the regulatory-side mandate.

TypeDirect peer
Description

UK Arm's Length Body that processes NHS prescription pricing, reimburses community pharmacies, and supports drug tariff management. Comparable to NPPA in operating the financial/reimbursement backbone of a public drug-pricing system.

TypeBroad incumbent
Description

US federal agency administering Medicare/Medicaid, including drug pricing programmes (e.g., Inflation Reduction Act negotiation). Comparable as the US government's primary payer-side pharmaceutical price regulator; operates at much larger scale but with analogous tools (ceiling pricing, negotiation, programme compliance).

TypeDirect peer
Description

India's counterpart drug regulator under the Ministry of Health & Family Welfare; oversees drug safety, approvals, and clinical trials. Sister federal regulator to NPPA with overlapping data and stakeholder relationships, though focused on safety rather than pricing.

TypeDirect peer
Description

New Zealand's crown entity that decides which medicines are subsidised and negotiates/regulates their pricing. Closely comparable in combining price regulation, formulary decision-making, and direct public-health impact via affordability.

TypeBroad incumbent
Description

EU-level medicines regulator coordinating drug approvals across member states. Larger, supranational incumbent with safety/efficacy focus but engages with HTA bodies on pricing and reimbursement evidence requirements.

TypeBroad incumbent
Description

UK's national regulator for medicines, medical devices, and blood components. Comparable as a national statutory medicines regulator; broader remit than NPPA but same federal-regulator archetype.

TypeDirect peer
Description

Canada's federal drug price regulator with a near-identical mandate: setting ceiling prices for patented medicines and protecting consumers from excessive pricing. Most directly comparable single-function drug price regulator to NPPA.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

National Pharmaceutical Pricing Authority

Pharmaceutical Price Regulationnppa.gov.in

National Pharmaceutical Pricing Authority is the sole statutory regulator of pharmaceutical and medical device pricing in India, operating under the Department of Pharmaceuticals to fix ceiling prices, monitor compliance, and serve citizens, manufacturers, and government health schemes via IPDMS 2.0 and a 32-State PMRU network.

What National Pharmaceutical Pricing Authority does

National Pharmaceutical Pricing Authority (NPPA) is a statutory regulatory authority constituted by Government of India Resolution on 29 August 1997 and attached to the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers. It functions as the sole independent regulator for pharmaceutical pricing in India under the Essential Commodities Act, 1955 and the Drugs (Price Control) Order, 2013, fixing and revising ceiling prices for scheduled formulations and retail prices for new drugs.

NPPA operates three core digital and physical platforms: the Integrated Pharmaceutical Database Management System (IPDMS 2.0), which captures production, import, export, market share, and profitability data from manufacturers across bulk drugs and formulations; the Pharma Sahi Daam App/Portal, a consumer-facing tool for verifying ceiling prices and filing overcharging grievances; and the Price Monitoring and Research Units (PMRUs), field offices in 32 State/UTs that execute monitoring, public awareness, and enforcement. Ceiling prices have been issued for 928 scheduled formulations and retail prices for approximately 3,111 new drugs. Price regulation has been extended into medical devices (coronary stents, knee implants, anti-rabies immunoglobulin, IV fluids) and, in public-interest interventions under Para 19 of DPCO 2013, into 106 anti-diabetic and cardiovascular drugs and 42 anti-cancer drugs (the latter generating reported savings of up to 90%, or Rs. 984 crores per annum, across 526 brands).

NPPA does not generate commercial revenue. It is wholly funded through Government of India budget allocations and does not charge for regulatory services. Its "customers" in the functional sense are Indian citizens and patients (beneficiaries of price control), pharmaceutical manufacturers and distributors (regulated entities filing Form IV and pricing submissions through IPDMS 2.0), State Drug Controllers (enforcement network), and government health schemes such as Ayushman Bharat. Leadership comprises a Chairman, Member Secretary, and authority members drawn from CDSCO, the Department of Expenditure (Chief Adviser - Cost), and the Department of Economic Affairs (Economic Adviser).

National Pharmaceutical Pricing Authority firmographics

Firmographics
Name
National Pharmaceutical Pricing Authority
Legal name
National Pharmaceutical Pricing Authority
Website
https://nppa.gov.in
Company type
Private
Founded year
1997
Operating status
Operating
Short description
National Pharmaceutical Pricing Authority is the sole statutory regulator of pharmaceutical and medical device pricing in India, operating under the Department of Pharmaceuticals to fix ceiling prices, monitor compliance, and serve citizens, manufacturers, and government health schemes via IPDMS 2.0 and a 32-State PMRU network.
Ownership category
akta.pro rank

National Pharmaceutical Pricing Authority industry classification

Industry
Product category
Pharmaceutical Price Regulation
akta.pro primary industry
Drug Regulators (Human Pharmaceuticals) (HLAJADAA)
akta.pro secondary industry
Government Pricing & Compliance (Medicare/Medicaid/340B/AMP/Best Price) (HLAIAKAE)

Keywords

  • Drug price regulation
  • Pharmaceutical pricing
  • Ceiling price fixation
  • Medicine affordability
  • Pharmaceutical policy

Where National Pharmaceutical Pricing Authority is headquartered

Location

Headquarters

HQ city
New Delhi
HQ country
India
HQ region
Asia

Markets served

National Pharmaceutical Pricing Authority business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Technology or R&D, Infrastructure, Others

Distribution channels3 records

Marketing channels4 records

National Pharmaceutical Pricing Authority product offering

Product offering

Core offering

National Pharmaceutical Pricing Authority (NPPA) is the statutory regulator for pharmaceutical pricing in India, constituted in 1997 under the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers. It fixes and revises ceiling prices for drugs notified under Schedule-I of the Drugs (Price Control) Order (DPCO) 2013, provides retail prices for new drugs, regulates prices of medical devices (coronary stents, knee implants), and operates digital platforms (IPDMS 2.0 and Pharma Sahi Daam) plus a 32-state PMRU network to monitor compliance, prevent overcharging, and ensure affordable access to essential medicines.

Product overview

NPPA operates as a regulatory body rather than a commercial product company. Its primary digital offerings include the Pharma Sahi Daam App/Portal for consumer price verification and grievance registration, the Integrated Public Database Management System (IPDMS) 2.0 for pharmaceutical data management, and a network of Price Monitoring and Research Units (PMRUs) across 32 states. These work together as part of the CAPPMS framework to regulate and monitor drug prices, ensure availability of affordable medicines, and handle public complaints.

Differentiator

Problem solved

Functional benefit

Brands

  • Pharma Sahi Daam: A platform/app for information on medicine prices and registering public grievances.
  • IPDMS 2.0
  • PMRU

Products and services

  • Pharma Sahi Daam App/Portal Mobile app and web portal that enables consumers to verify ceiling prices of scheduled medicines and register public grievances about overcharging by pharmaceutical companies or retailers. Built for Indian citizens seeking price transparency for essential and life-saving medicines.
  • Integrated Pharmaceutical Database Management System (IPDMS) 2.0 Comprehensive digital platform for managing, regulating, and monitoring prices of pharmaceutical products and medical devices. Enables online information collection from pharmaceutical manufacturers and serves as a significant step towards enhancing transparency, efficiency, and accountability in the pharmaceutical and medical devices sector. Used by pharmaceutical manufacturers for compliance submissions.
  • Price Monitoring and Research Units (PMRUs) State/UT-level field units for strengthening monitoring, public awareness, and enforcement of drug pricing regulations across India. Currently operational in 32 State/UTs as NPPA's decentralized enforcement and outreach arm.
  • CAPPMS (Consumer Awareness, Price Monitoring and Public Grievance System) Integrated framework for consumer awareness on drug pricing, monitoring of pharmaceutical prices, and handling of public grievances. Operates through PMRUs across states and integrates with the Pharma Sahi Daam portal and IPDMS 2.0.

Companies that use National Pharmaceutical Pricing Authority

Customer profile

Segments3 records

Ideal customer profiles3 records

National Pharmaceutical Pricing Authority technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

National Pharmaceutical Pricing Authority partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered core and minor.

  • Department of Pharmaceuticals (DoP), Ministry of Chemicals & Fertilizers, Government of IndiacoreOthersNPPA is an attached office of the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers. It implements the National Pharmaceutical Pricing Policy, 2012 and the Drugs (Price Control) Orders issued by DoP. Powers are delegated to NPPA for fixing and revising drug prices as per DPCO provisions.
  • Drug Controller General of India (CDSCO), Ministry of Health and Family WelfarecoreStrategic or Co-development PartnerCollaboration with CDSCO for integrated data collection, regulation, and improved services. Dr. Rajeev Singh Raghuvanshi serves as Drugs Controller General of India and is a member of NPPA Authority.
  • Price Monitoring and Research Units (PMRUs) in 32 State/UTscoreOthersPMRUs established at State/UT levels for strengthening, monitoring and public awareness on drug pricing. NPPA is expanding outside Delhi through these units.
  • NIPERs (National Institutes of Pharmaceutical Education and Research)minorStrategic or Co-development PartnerNPPA seeks to synergize with NIPERs for integrated data collection and undertake concurrent research and studies to enable credible contribution to policy development.
  • State Drug ControllerscoreStrategic or Co-development PartnerNPPA collaborates with State Drug Controllers for integrated data collection, regulation, and improved services to the people. State Drug Controllers are listed as related entities on NPPA website.
  • Department of Expenditure, Ministry of FinancecoreOthersAnand Kumar Pal, Chief Adviser (ICoAS) from the Office of Chief Adviser (Cost), Department of Expenditure, serves as a member of NPPA Authority.
  • Department of Economic Affairs, Ministry of FinancecoreOthersDr. Rose Mary K. Abraham, Economic Adviser from Department of Economic Affairs, serves as a member of NPPA Authority.
  • Pharmaceutical ManufacturersminorOthersPharmaceutical manufacturers operating in India who submit pricing data through IPDMS 2.0 and comply with DPCO regulations. Estimated over 60,000 medicines sold by over 2,30,000 retail chemists in trade channel.

Scale indicators6 records

Recent moves7 records

Expansion highlights6 records

National Pharmaceutical Pricing Authority competitors and assessment

Company assessment

Others

  • IQVIA: Global pharmaceutical data, analytics, and consulting provider. Comparable on the data-infrastructure layer NPPA relies on (IPDMS 2.0), but as an enabling technology vendor rather than a regulatory peer.

Broad incumbents

  • US Food and Drug Administration (FDA): The US federal regulator for drugs, biologics, medical devices, and food. A broader incumbent in the same regulatory space; FDA also engages in pricing-adjacent work through Centers for Medicare & Medicaid Services, though its core mandate is safety and efficacy rather than price.
  • Therapeutic Goods Administration (TGA, Australia): Australia's regulator for therapeutic goods including medicines and medical devices. Broader incumbent in the same regulatory family; pricing happens separately via the Pharmaceutical Benefits Scheme, so TGA is most comparable on the regulatory-side mandate.
  • Centers for Medicare & Medicaid Services (CMS): US federal agency administering Medicare/Medicaid, including drug pricing programmes (e.g., Inflation Reduction Act negotiation). Comparable as the US government's primary payer-side pharmaceutical price regulator; operates at much larger scale but with analogous tools (ceiling pricing, negotiation, programme compliance).
  • European Medicines Agency (EMA): EU-level medicines regulator coordinating drug approvals across member states. Larger, supranational incumbent with safety/efficacy focus but engages with HTA bodies on pricing and reimbursement evidence requirements.
  • Medicines and Healthcare products Regulatory Agency (MHRA): UK's national regulator for medicines, medical devices, and blood components. Comparable as a national statutory medicines regulator; broader remit than NPPA but same federal-regulator archetype.

Direct peers

  • NHS Business Services Authority (NHSBSA): UK Arm's Length Body that processes NHS prescription pricing, reimburses community pharmacies, and supports drug tariff management. Comparable to NPPA in operating the financial/reimbursement backbone of a public drug-pricing system.
  • Central Drugs Standard Control Organisation (CDSCO): India's counterpart drug regulator under the Ministry of Health & Family Welfare; oversees drug safety, approvals, and clinical trials. Sister federal regulator to NPPA with overlapping data and stakeholder relationships, though focused on safety rather than pricing.
  • Pharmaceutical Management Agency (PHARMAC): New Zealand's crown entity that decides which medicines are subsidised and negotiates/regulates their pricing. Closely comparable in combining price regulation, formulary decision-making, and direct public-health impact via affordability.
  • Patented Medicine Prices Review Board (PMPRB): Canada's federal drug price regulator with a near-identical mandate: setting ceiling prices for patented medicines and protecting consumers from excessive pricing. Most directly comparable single-function drug price regulator to NPPA.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat3 records

Key risks6 records

Key highlights6 records

Customer concentration

National Pharmaceutical Pricing Authority social profiles

Digital presence

National Pharmaceutical Pricing Authority financial estimates

Financial estimate

Revenue estimate

Valuation estimate

National Pharmaceutical Pricing Authority leadership team

Management profile

Number of profiles

Profiles1 record

National Pharmaceutical Pricing Authority funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

National Pharmaceutical Pricing Authority M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about National Pharmaceutical Pricing Authority

What does National Pharmaceutical Pricing Authority do?

National Pharmaceutical Pricing Authority (NPPA) is the statutory regulator for pharmaceutical pricing in India, constituted in 1997 under the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers. It fixes and revises ceiling prices for drugs notified under Schedule-I of the Drugs (Price Control) Order (DPCO) 2013, provides retail prices for new drugs, regulates prices of medical devices (coronary stents, knee implants), and operates digital platforms (IPDMS 2.0 and Pharma Sahi Daam) plus a 32-state PMRU network to monitor compliance, prevent overcharging, and ensure affordable access to essential medicines.

Is National Pharmaceutical Pricing Authority a public or private company?

National Pharmaceutical Pricing Authority is a private company. It is classified as state government owned and is currently operating.

When was National Pharmaceutical Pricing Authority founded?

National Pharmaceutical Pricing Authority was founded in 1997.

Where is National Pharmaceutical Pricing Authority based?

National Pharmaceutical Pricing Authority is headquartered in New Delhi, India, in the Asia region.

Who are National Pharmaceutical Pricing Authority's main competitors?

IQVIA is listed as an others. Broad incumbents are US Food and Drug Administration (FDA), Therapeutic Goods Administration (TGA, Australia), Centers for Medicare & Medicaid Services (CMS), European Medicines Agency (EMA) and Medicines and Healthcare products Regulatory Agency (MHRA). Direct peers are NHS Business Services Authority (NHSBSA), Central Drugs Standard Control Organisation (CDSCO), Pharmaceutical Management Agency (PHARMAC) and Patented Medicine Prices Review Board (PMPRB).

Does National Pharmaceutical Pricing Authority have an API?

No public API is recorded for National Pharmaceutical Pricing Authority.

What industry is National Pharmaceutical Pricing Authority in?

National Pharmaceutical Pricing Authority's product category is Pharmaceutical Price Regulation. Its primary akta.pro industry code is HLAJADAA, Drug Regulators (Human Pharmaceuticals), with a secondary code of HLAIAKAE, Government Pricing & Compliance (Medicare/Medicaid/340B/AMP/Best Price).

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Live signals
CNBCTV18Why a 30% cancer drug margin cap could hurt hospital earnings - CNBC TV18Macquarie Capital warns a proposed 30% cap on non-scheduled cancer drug margins could cut Max Healthcare's EBITDA by mid-teens and Apollo Hospitals' by high single digits. The National Pharmaceutical Pricing Authority cites an average 170% mark-up, and a Supreme Court hearing on Oct 12 could influence intervention.The Times of IndiaDrug cos refuse to take sole responsibility for overpricingPharmaceutical groups, including FOPE, have objected to a National Pharmaceutical Pricing Authority proposal that would make manufacturers solely responsible for drug overpricing. They argue retailers and hospitals share liability under the DPCO, and urged a transition period and protection for downstream sellers.The Times of IndiaDrugmakers may bear sole responsibility for overpricing essential medicines under NPPA proposalThe National Pharmaceutical Pricing Authority has proposed deleting a Drug Price Control Order 2013 provision that allowed action against retailers and hospitals found knowingly selling overpriced medicines, leaving manufacturers solely liable. Industry sources expect manufacturers to contest the move. The watchdog has levied ₹8,447 crore in penalties through March 2026, recovering ₹1,582 crore from drugmakers across 2,737 cases.The Times of IndiaDrugmakers may bear sole responsibility for overpricing essential medicines under NPPA proposalThe National Pharmaceutical Pricing Authority proposed deleting a clause that allows action against retailers who knowingly sell overpriced essential medicines, leaving drugmakers solely responsible. Industry sources oppose the move, citing unfairness. The watchdog has filed 2,737 pricing violation cases and recovered ₹1,582 crore from drugmakers.ScanXDelhi High Court stays NPPA overcharging notice against AstraZeneca until 2027The Delhi High Court stayed a demand notice issued by the National Pharmaceutical Pricing Authority against AstraZeneca Pharma India over alleged overcharging of Betaloc-50, effective until February 10, 2027. The regulator claimed the company failed to implement revised ceiling prices notified in March and June 2016 under the Drugs (Prices Control) Order, 2013. AstraZeneca must deposit 15% of the demanded amount with the court registrar.Telegraph IndiaMedical device prices in India up to 25 times cost AIMED urges govt to cap margins - Telegraph IndiaThe Association of Indian Medical Devices (AIMED) has urged the Indian government to regulate trade margins and cap maximum retail prices for medical devices, citing instances where patients pay up to 25 times the factory cost. AIMED argues that manufacturers are forced to inflate prices to sustain margins for hospitals and retailers, which distorts competition with imported devices dominating the market. The industry body has proposed specific margin caps to different device categories and is seeking intervention from the Department of Pharmaceuticals and the National Pharmaceutical Pricing Authority.MedicaldialoguesSame Drug, Different Brand, Different MRP? Centre Explains Pricing Rules Under DPCOThe Indian Government clarified that medicines with identical active ingredients can legally carry different Maximum Retail Prices (MRPs) under different brand names, provided they remain within the ceiling prices set by the National Pharmaceutical Pricing Authority (NPPA). This explanation was provided in Parliament to address concerns about price variations while highlighting that out-of-pocket healthcare expenditure has significantly declined from 62.6% in 2014-15 to 43.4% in 2022-23 due to existing pricing regulations and public health initiatives.The HinduWhy vital chemotherapy drugs are in short supply in IndiaIndia is experiencing a critical nationwide shortage of chemotherapy drugs cisplatin and carboplatin due to soaring global platinum costs and shipping disruptions. In response, the National Pharmaceutical Pricing Authority (NPPA) raised price caps by 50% to incentivize domestic manufacturers to restart halted production lines. While government hospitals have largely stabilized supplies through existing stocks or tenders, private hospitals face ongoing crunches causing treatment delays for patients.FmiblogCoronary Stents Market in India: NPPA Price ImpactIndia’s National Pharmaceutical Pricing Authority (NPPA) has imposed price caps on coronary stents, setting ceilings at Rs 7,260 for bare metal stents and Rs 29,600 for drug-eluting stents. This regulatory intervention aims to improve affordability by significantly reducing prices from previous ranges of up to Rs 1.5 lakh, though it faces opposition from manufacturers concerned about impacts on innovation and margins. The decision marks a structural shift in the Indian medical device market, which was valued at US$531 million in 2016.Ani NewsParliamentary panel seeks review of extant categorization of medicines to plug any arbitrary fixation in prices of non-scheduled formulationsA Parliamentary Standing Committee on Chemicals and Fertilizers has recommended a comprehensive review of the pricing framework for non-scheduled medicines in India, noting that approximately 82% of the pharmaceutical market comprises formulations whose prices are set by manufacturers themselves. The committee has urged the Department to examine reintroducing cost-based pricing mechanisms through statutory amendments wherever significant price disparities or abnormally high mark-ups are observed, and called for finalizing a permanent Trade Margin Rationalisation framework within the DPCO, 2013. The recommendations, part of the 33rd Report on the role and functions of the National Pharmaceutical Pricing Authority (NPPA), were presented in the Lok Sabha.