Health

Inhalers

Asthma and COPD inhaled therapies.

Why it matters · Therapeutic switching and out-of-pocket cost pressure.

12

Inputs

21

Companies

8

Facilities

10

Source countries

How it's made

The process

  1. 01

    API Synthesis & Micronization

    Chemical synthesis of active bronchodilator or anti-inflammatory compounds: salbutamol, budesonide, fluticasone, tiotropium, formoterol. pMDI-grade APIs require micronization to 1–5 µm MMAD for lung deposition. DPI APIs may be micronized or spray-dried. Dominated by a small number of innovator facilities (GSK Montrose, AstraZeneca Södertälje) and generic manufacturers concentrated in India (Cipla) and China.

  2. 02

    Formulation Development and Drug-Excipient Blending

    For pMDIs: micronized API suspended or dissolved in HFA propellant (HFA-134a or HFA-227ea) with co-solvents and surfactants. Formulation is locked at development — propellant changes require full regulatory resubmission. For DPIs: API blended with inhalation-grade carrier lactose (Meggle InhaLac or DFE Pharma Lactohale) in precise mass ratios under controlled humidity. Changing lactose grade requires complete clinical bridging studies.

  3. 03

    Canister and Valve Component Manufacturing

    For pMDIs: aluminum canisters deep-drawn from aluminum slugs, then internally coated (PTFE/plasma treatment) to prevent drug adsorption. H&T Presspart claims components in ~85% of global MDIs. Metering valves (25–100 µL per actuation) produced separately by Bespak (King's Lynn) or Aptar Pharma (Le Vaudreuil). For DPIs: device housings and powder reservoirs injection-molded using pharmaceutical-grade polymers by device specialists (Plastiape, Recipharm).

  4. 04

    HFA Propellant Production and Purification

    HFA-134a and HFA-227ea synthesized via fluorochemical processes from fluorspar and hydrofluoric acid. Pharmaceutical-grade propellant requires purity >99.99% with tightly controlled moisture and residual solvent specs. Koura (Runcorn, UK) supplies ~75% of global pMDI propellant under its Zephex brand and is the only FDA-registered active supplier in the US. A new low-GWP era begins: Koura's HFA-152a facility (GWP=4) opened March 2022; AstraZeneca and Chiesi are in Phase III trials with HFO-1234ze.

  5. 05

    Pressurized Fill and Finish (pMDI) or Powder Filling (DPI)

    For pMDIs: canister, valve, and formulation assembled under pressure in pharmaceutical-grade cleanrooms. Propellant filled under pressure at -40°C or via pressure-filling at ambient temperature; each canister 100% weight-checked. For DPIs: pre-blended powder filled into device reservoirs or unit-dose capsules/blisters in low-humidity (<40% RH) cleanrooms. CDMOs with this capability include Recipharm (Holmes Chapel), Catalent (Morrisville NC), and Bespak. Very few globally qualified facilities.

  6. 06

    Actuator and Device Assembly

    Filled pMDI canisters inserted into molded plastic actuators (mouthpieces with nozzle orifices sized for spray geometry). For DPIs, proprietary device platforms (Turbuhaler, Ellipta, Diskus, HandiHaler, Breezhaler, RS01) are fully assembled and checked for inspiratory-flow triggering. Dose counter mechanisms added. All assembly in ISO 7–8 cleanrooms.

  7. 07

    Quality Control Testing and Release

    Every batch undergoes cascade impactor testing to verify aerodynamic particle size distribution and fine particle fraction; leak testing; dose content uniformity testing across device life; valve delivery testing; microbial testing. USP 601, Ph.Eur. 2.9.18, and product-specific FDA/EMA guidances apply. Failed batches cannot be reworked — contents must be destructively disposed. Batch release takes 2–6 weeks.

  8. 08

    Packaging and Distribution (Dangerous Goods)

    Finished inhalers packaged with patient information leaflets and spacer devices. pMDIs classified as dangerous goods under IATA/IMDG (pressurized flammable propellant) — restricts air cargo quantities and adds logistics cost. Global serialization requirements (US DSCSA, EU FMD) add tracking overhead. Branded inhalers distributed through national pharmaceutical wholesalers; generics through parallel trade channels in EU.

Where it comes from

Country dependencies

Weighted share of upstream inputs sourced from each country.

CountryWeighted shareInputs supplied to inhalers
GBUnited Kingdom47%HFA-134a Propellant (Norflurane) · pMDI Aluminum Canister (Coated) · pMDI Metering Valve +1
JPJapan45%Vibrating Mesh Membrane (Nebulizer)
INIndia45%Salbutamol (Albuterol) API
DEGermany43%Inhalation-Grade Lactose Monohydrate · Vibrating Mesh Membrane (Nebulizer)
MXMexico32%HFA-134a Propellant (Norflurane) · Hydrofluoric Acid (Anhydrous HF)
FRFrance25%Hydrofluoric Acid (Anhydrous HF) · pMDI Metering Valve
NLNetherlands22%Inhalation-Grade Lactose Monohydrate · Vibrating Mesh Membrane (Nebulizer)
CNChina20%HFA-134a Propellant (Norflurane) · Hydrofluoric Acid (Anhydrous HF) · pMDI Aluminum Canister (Coated) +1
USUnited States11%HFA-134a Propellant (Norflurane) · Hydrofluoric Acid (Anhydrous HF)
ITItaly10%pMDI Aluminum Canister (Coated) · pMDI Metering Valve

Who makes it

Supplier companies

21 companies in this supply chain, sorted by market share.

H&T Presspart
HQ GB85% share

Subsidiary of H&T Group. World's leading manufacturer of aluminum MDI canisters and plastic actuator components. Claims components used in 85% of global MDIs. Operates the Inhalation Product Technology Centre (IPTC) at Blackburn, UK for low-GWP propellant development.

Supplies these inputs

pMDI Aluminum Canister (Coated)

Replaceability

Substitutability 10% · 36 mo to replace

Business segments

  • pMDI Aluminum Canisters (World #1 — 85% global share)70% rev
  • pMDI Plastic Actuators & Dose Counters20% rev
  • Low-GWP Propellant Transition (IPTC)10% rev

Division of Orbia (formerly Mexichem). World leader in pharmaceutical-grade HFA propellants under the Zephex brand. Zephex 134a in ~75% of global pMDIs. Only FDA-registered active HFA-134a supplier in the US. Opened world's first commercial HFA-152a pharmaceutical manufacturing facility at Runcorn, UK in March 2022.

Supplies these inputs

HFA-134a Propellant (Norflurane) · HFA-227ea Propellant (Apaflurane) · Hydrofluoric Acid (Anhydrous HF)

Replaceability

Substitutability 15% · 18 mo to replace

Business segments

  • Pharmaceutical HFA Propellants (Zephex Brand)35% rev
  • Industrial & HVAC Fluorochemicals40% rev
  • Orbia Parent (Mexichem Heritage)25% rev
Bespak
HQ GB45% share

World's leading pMDI metering valve supplier. Its BK357 valve platform is used in more pMDI products globally than any other. Also provides CDMO fill-finish services for pMDIs and DPIs. Partnered with H&T Presspart on sustainable pMDI supply chain transition.

Supplies these inputs

pMDI Metering Valve

Replaceability

Substitutability 10% · 36 mo to replace

Business segments

  • pMDI Metering Valves (World #1 — BK357 Platform)55% rev
  • CDMO Services (pMDI + DPI Fill-Finish)30% rev
  • Consumer & Industrial Aerosol Valves15% rev
DFE Pharma
HQ NL40% share

Specialty pharmaceutical-grade lactose company (HQ Goch, Germany; joint venture between Fonterra Co-operative Group and FrieslandCampina); the world's largest producer of pharmaceutical-grade lactose for use as a drug excipient in tablets, capsules, and dry powder inhalers. DFE Pharma's lactose (Pharmatose® brand) is used in the vast majority of pharmaceutical tablet and capsule formulations globally — most pills you take contain DFE Pharma lactose as a filler, flow agent, or binder. DFE Pharma's manufacturing combines Fonterra (NZ) lactose raw material expertise with FrieslandCampina (NL) processing capability. The same Fonterra-FrieslandCampina lactose joint venture that makes the excipient in most of the world's pharmaceutical tablets also produces food-grade lactose for infant formula.

Supplies these inputs

Inhalation-Grade Lactose Monohydrate

Replaceability

Substitutability 10% · 60 mo to replace

Business segments

  • Oral Solid Dose Lactose Excipients (Pharmatose Brand)55% rev
  • Inhalation-Grade Lactose (Inhalac Brand)30% rev
  • Dairy Ingredients (Fonterra/FrieslandCampina Heritage)15% rev
Meggle Pharma
HQ DE40% share

German dairy and pharmaceutical excipient company. Through its InhaLac product line, one of two dominant global suppliers of inhalation-grade lactose monohydrate for DPI formulations. Inhalation lactose is a high-value niche — technically demanding particle size engineering from dairy lactose.

Supplies these inputs

Inhalation-Grade Lactose Monohydrate

Replaceability

Substitutability 10% · 60 mo to replace

Business segments

  • InhaLac (Inhalation-Grade Lactose) — World #130% rev
  • Oral Solid Dose Pharmaceutical Excipients25% rev
  • Dairy Ingredients & Food (MEGGLE parent)45% rev

Japanese healthcare equipment company (OMRON Corporation subsidiary; HQ Muko, Kyoto Prefecture; OMRON Corporation TSE: 6645); makes mesh nebulizers (MicroAIR NE-U22 series) and manufactures vibrating mesh membranes in-house using precision photo-etching and electroforming processes at its Japanese manufacturing facilities. OMRON Healthcare is the world's leading mesh nebulizer manufacturer by volume, and its MicroAIR technology uses titanium or stainless steel mesh membranes with 2,700-6,000 holes of 2.1-5.7 μm diameter, produced using semiconductor-grade precision etching processes. OMRON is a Japanese industrial conglomerate whose products span: industrial automation robots (the largest revenue segment), healthcare monitors (blood pressure monitors, thermometers, glucose meters), and drug delivery devices (nebulizers). The same OMRON that makes blood pressure cuffs sold at CVS also makes the precision titanium mesh through which albuterol passes in a hospital ICU nebulizer therapy session.

Supplies these inputs

Vibrating Mesh Membrane (Nebulizer)

Replaceability

Substitutability 25% · 24 mo to replace

Business segments

  • Industrial Automation Business (IAB)47% rev
  • Healthcare Business (HCB)23% rev
  • Social Systems Solutions & Service (SSB)16% rev
  • Electronic & Mechanical Components (EMC)14% rev
Aptar Pharma (ATR)
HQ US35% share

American drug delivery and packaging company (NYSE: ATR, HQ Crystal Lake IL; ~$3.5B revenue); Aptar Pharma division produces drug delivery devices and components including injectable drug delivery systems, needle-free injection components, and parenteral packaging. For IV bag applications, Aptar supplies injection site components and additive port systems. Aptar also produces metered-dose inhaler (MDI) valves for asthma inhalers (a major product line), nasal spray pumps, and eye dropper closures. The same Aptar company that makes the pumping mechanism in your nasal allergy spray also supplies components for IV bag injection ports.

Supplies these inputs

pMDI Metering Valve

Replaceability

Substitutability 10% · 36 mo to replace

Business segments

  • Pharmaceutical Drug Delivery Devices38% rev
  • Beauty, Home & Personal Care (Consumer)42% rev
  • Food & Beverage Dispensing20% rev
GSK (GSK)
HQ GB30% share

UK pharmaceutical company; sole manufacturer and formulator of AS01B adjuvant system (QS-21 + MPL in liposomes); used in Shingrix (herpes zoster vaccine, $4B+ annual revenue) and RTS,S/Mosquirix (malaria vaccine); retaining AS01E adjuvant supply even as malaria vaccine manufacturing transfers to Bharat Biotech

Supplies these inputs

Salbutamol (Albuterol) API

Replaceability

Substitutability 35% · 18 mo to replace

Business segments

  • Respiratory Inhalers (Ventolin, Advair, Trelegy)35% rev
  • Vaccines (Shingrix, Flu, Mosquirix)40% rev
  • Specialty Medicines (HIV, Oncology, Rare Disease)25% rev

German respiratory medical device company (HQ Starnberg, Bavaria; private, founded 1906); a specialist inhaler and nebulizer manufacturer whose eFlow® technology (LC Sprint nebulizer, eFlow rapid) uses vibrating perforated membranes to generate pharmaceutical aerosols without heating the drug. PARI's eFlow mesh nebulizers are used for inhalation of antibiotics (tobramycin for cystic fibrosis — Cayston via Altera nebulizer), colistin, and experimental therapies where drug stability limits pMDI use. PARI manufactures its vibrating mesh membranes through European precision metalworking partnerships. PARI was founded in 1906 (pre-World War I) in Munich as an atomizer manufacturer — making it one of the oldest respiratory drug delivery device companies in the world. PARI's nebulizers are the device of choice for cystic fibrosis patients requiring daily antibiotic inhalation therapy — a demanding use case where mesh membrane longevity and aerosol consistency are life-critical.

Supplies these inputs

Vibrating Mesh Membrane (Nebulizer)

Replaceability

Substitutability 25% · 24 mo to replace

Business segments

  • Mesh Nebulizer Systems (eFlow)55% rev
  • Jet Nebulizer Systems30% rev
  • Pharmaceutical Partnerships & Licensing10% rev
  • Veterinary & Research Nebulizers5% rev

Dutch healthcare technology company (Euronext: PHIA, HQ Amsterdam; ~$18B revenue); Respironics division (acquired from Respironics Inc. 2008) produces mesh nebulizers (InnoSpire Go, SideStream) as part of its respiratory care portfolio. Philips Respironics was severely damaged by the 2021 recall of ~4 million CPAP machines (Continuous Positive Airway Pressure for sleep apnea) due to sound abatement foam that was found to degrade into potentially carcinogenic particles — the largest medical device recall in US history by value (~$1.5B settlement, regulatory sanctions, CEO resignation). The Philips CPAP recall, while unrelated to its nebulizer products, significantly damaged the company's reputation, financial position, and regulatory standing — creating uncertainty about its nebulizer product line continuity. A CPAP foam degradation problem in sleep apnea devices created supply chain uncertainty for mesh nebulizers used by hospital COPD patients.

Supplies these inputs

Vibrating Mesh Membrane (Nebulizer)

Replaceability

Substitutability 25% · 24 mo to replace

Business segments

  • Diagnosis & Treatment45% rev
  • Connected Care30% rev
  • Personal Health25% rev
Solvay (SOLB.BR)
HQ BE18% share

Belgian specialty chemical company (Euronext: SOLB, HQ Brussels; ~€4.9B revenue after 2023 split); major global HF (hydrogen fluoride) producer and the world's largest producer of fluorine-based specialty chemicals. Solvay's HF is produced at multiple European sites (Dombasle-sur-Meurthe, France; Rosignano, Italy) via reaction of fluorspar (CaF2) with sulfuric acid. HF is the gateway chemical for Solvay's entire fluorine chemistry chain: HF → fluoropolymers (PTFE, PVDF), refrigerants (HFCs/HFOs), specialty fluorinated gases (NF3 precursor), and electronic-grade HF for semiconductors. Solvay split into two companies in December 2023 — the new 'Solvay' retained the specialty chemicals (including HF and fluorine) while 'Syensqo' retained the advanced materials — so the HF supply chain is now within the post-split Solvay entity. Solvay was founded in 1863 by Ernest Solvay, inventor of the Solvay process for soda ash (sodium carbonate) production — the same Belgian industrial dynasty that revolutionized 19th-century chemical manufacturing now controls a critical node in 21st-century semiconductor supply chains.

Supplies these inputs

Hydrofluoric Acid (Anhydrous HF)

Replaceability

Substitutability 30% · 18 mo to replace

Business segments

  • Soda Ash & Sodium Bicarbonate (Heritage Business)35% rev
  • HF & Fluorine Chemicals (Gateway to Semiconductor Supply Chain)30% rev
  • Silica & Specialty Materials (Now Syensqo Post-Split)20% rev
  • Peroxides & Oxygenated Products15% rev
Cipla (CIPLA)
HQ IN15% share

Indian generic pharmaceutical company and the world's largest generic inhaler manufacturer by volume. Pioneer of generic salbutamol inhalers in India (1978). Manufactures generic pMDIs at scale. Received FDA final approval for generic Proventil HFA. Critical supplier during COVID-19 when global inhaler demand surged.

Supplies these inputs

Salbutamol (Albuterol) API

Replaceability

Substitutability 40% · 12 mo to replace

Business segments

  • Generic Respiratory Inhalers (pMDI + DPI)35% rev
  • HIV/ARV and Infectious Disease Generics25% rev
  • Branded Generics (India) + Oncology40% rev

American industrial conglomerate (Nasdaq: HON, HQ Charlotte NC; ~$36B revenue); Advanced Materials division produces HF and a range of fluorinated specialty chemicals at Geismar Louisiana (one of the world's largest HF and fluoropolymer production sites). Honeywell's Geismar LA facility is a major supplier of HF to industrial and specialty chemical markets, as well as fluorinated refrigerants (Solstice series HFOs) and NF3 precursor HF. Honeywell's fluorine chemistry heritage traces to AlliedSignal (merged with Honeywell 1999) which itself acquired the fluorine chemistry business of Allied Chemical — which owned the original US fluorspar-to-HF process patents dating to the Manhattan Project era, when HF was needed for uranium enrichment (UF6 gaseous diffusion). The same US HF production infrastructure built for nuclear weapons development now supplies semiconductor-grade fluorinated gases.

Supplies these inputs

Hydrofluoric Acid (Anhydrous HF)

Replaceability

Substitutability 30% · 18 mo to replace

Business segments

  • Hydrogen Fluoride (HF) Production30% rev
  • Semiconductor Process Gases (NF3, WF6)25% rev
  • HFO Refrigerants (Solstice Series)30% rev
  • Fluoropolymers & Specialty Chemicals

American industrial conglomerate (Nasdaq: HON, HQ Charlotte NC; ~$36B revenue); Performance Materials and Technologies division produces HFA-134a refrigerant and pharmaceutical-grade propellant, as well as next-generation low-GWP alternatives including Solstice® HFO-1234yf (automotive AC replacement) and HFA-152a (low-GWP pMDI propellant for next-generation inhalers). Honeywell is developing pharmaceutical-grade HFA-152a as the primary replacement for HFA-134a in pMDIs as EU F-gas regulations phase down 134a — GWP of 152a is 4 vs 1,430 for 134a, meeting European climate targets. AstraZeneca, GlaxoSmithKline, and other pharma companies are partnering with Honeywell to develop and qualify HFA-152a-propelled inhalers for regulatory submission. Honeywell's position as both an HFA-134a producer AND a leading HFA-152a developer gives it a unique role in the regulatory transition threatening the current pMDI supply chain.

Supplies these inputs

HFA-134a Propellant (Norflurane)

Replaceability

Substitutability 20% · 36 mo to replace

Business segments

  • HFA-134a (pMDI Pharmaceutical Propellant)25% rev
  • HFA-152a (Next-Gen pMDI Propellant)15% rev
  • HFO Refrigerants (Solstice HVAC)40% rev
  • HFC Legacy & Specialty Gases

Italian specialty valve and actuator manufacturer (HQ Carnago, Varese, Lombardy; private, family-owned; ~€350M revenue); the third-tier supplier in pMDI metering valves behind Bespak and Aptar Pharma. Coster Group manufactures pMDI metering valves for generic inhaler manufacturers and some branded products, predominantly serving European and Latin American markets. Coster also manufactures aerosol valves for personal care products (hairspray, deodorant) and industrial applications — the same Italian valve engineering company that makes the valve in a can of Axe body spray also makes the metering valve that delivers albuterol in some generic asthma inhalers. Coster's position in the pMDI valve market represents a strategic supply diversification option for pharmaceutical companies seeking alternatives to the Bespak/Aptar duopoly, though its smaller scale and qualification breadth limits uptake.

Supplies these inputs

pMDI Metering Valve

Replaceability

Substitutability 10% · 36 mo to replace

Business segments

  • Personal Care & Household Aerosols60% rev
  • Pharmaceutical Aerosols20% rev
  • Food & Beverage Aerosols10% rev
  • Industrial & Technical Aerosols10% rev

Indian pharmaceutical company (NSE: SUNPHARMA, HQ Mumbai; ~₹600B revenue); world's fourth-largest specialty generic pharmaceutical company and India's largest pharma company by market cap. Sun Pharma manufactures salbutamol sulfate API and finished albuterol inhalers (pMDI and nebulizer solution) at multiple Indian manufacturing sites, supplying US and global generic markets through its Taro Pharmaceutical US subsidiary. Sun Pharma was founded in 1983 by Dilip Shanghvi, who started with just five pharmaceutical products and a single employee; today Sun Pharma employs 36,000 people and operates 43 manufacturing sites globally. Sun Pharma's founder Dilip Shanghvi is now one of India's wealthiest individuals — his journey from a $1M startup to a $30B market cap company in 40 years is one of the defining business stories of India's pharmaceutical sector rise.

Supplies these inputs

Salbutamol (Albuterol) API

Replaceability

Substitutability 35% · 18 mo to replace

Business segments

  • Generics (Respiratory/Inhalers)20% rev
  • Specialty Branded Pharmaceuticals30% rev
  • US Generic Pharmaceuticals (Taro)25% rev
  • Branded India & Emerging Markets25% rev

Teva Pharmaceutical Industries Ltd. (Tel Aviv Israel; NYSE: TEVA; ~$15.9B revenue 2023; world's largest generic pharmaceutical company by revenue) is a significant manufacturer and distributor of generic carboplatin injectable in the US market. Teva's API division (TAPI) and finished-dose operations supply generic oncology products including carboplatin to US hospital pharmacies. Teva experienced its own FDA enforcement actions in this period — in 2022, Teva's Irvine California facility was shut down due to contamination and sterilization failures, causing a separate streptozocin (pancreatic cancer drug) shortage. Teva's manufacturing is concentrated in Israel, India, and Eastern Europe, with US finished-dose manufacturing in North America. Teva's scale as the world's largest generic company makes it a critical backstop supplier when primary market participants face disruptions.

Supplies these inputs

Salbutamol (Albuterol) API

Replaceability

Substitutability 35% · 18 mo to replace

Business segments

  • Generic Injectables (Oncology)20% rev
  • Generic Respiratory (Inhalers)15% rev
  • Generic Oral & Solid Dose35% rev
  • Specialty Medicines20% rev
EMSAR S.r.l.
HQ IT8% share

Italian specialty pharmaceutical aerosol component manufacturer (HQ Senago, Milan; private); produces pharmaceutical-grade aluminum canisters for pMDI inhalers as one of the few alternatives to H&T Presspart. EMSAR serves primarily European generic inhaler manufacturers seeking second-source canister supply for risk mitigation. EMSAR's canister production is significantly smaller than H&T Presspart but provides a qualified alternative source for pharmaceutical companies willing to invest in dual-sourcing qualification programs. Italian precision manufacturing tradition in metalworking supports pharmaceutical-grade aluminum drawing operations.

Supplies these inputs

pMDI Aluminum Canister (Coated)

Replaceability

Substitutability 10% · 36 mo to replace

Business segments

  • Pharmaceutical Aerosol Canisters80% rev
  • Personal Care & Industrial Aerosol Canisters20% rev

Where it's made

Facilities

8 facilities producing inputs that feed inhalers.

Aptar Pharma Le Vaudreuil / Val-de-Reuil Operations

FR

Aptar Pharma · Normandy · Manufacturing

Key European manufacturing and R&D center for Aptar Pharma pMDI metering valves and nasal spray pumps. Manufactures DF30 valve platform for pMDI products.

Bespak King's Lynn Manufacturing Site

GB

Bespak · Norfolk, England · Manufacturing

Global headquarters and primary manufacturing site for BK357 and BK361 pMDI metering valves. Also houses CDMO fill-finish for pMDI and DPI. Bergen Way, North Lynn Industrial Estate, King's Lynn, Norfolk PE30 2JJ.

Cipla Goa Manufacturing Complex

IN

Cipla · Goa · Manufacturing

Key Cipla facility for respiratory pharmaceutical manufacturing including pMDI inhalers. Primary site for inhaler production for domestic and export markets. FDA-inspected facility.

DFE Pharma Borculo Inhalation Lactose Facility

NL

DFE Pharma · Gelderland · Manufacturing

Purpose-built pharmaceutical inhalation lactose production facility commissioned 2005. Acquired from Royal FrieslandCampina in 2010. Produces Lactohale inhalation-grade lactose lines. Needseweg 23, 7271 AB Borculo, Netherlands.

GSK Montrose API Manufacturing Site

GB

GSK · Angus, Scotland · Manufacturing

£110M dedicated API manufacturing facility for salbutamol (Ventolin active ingredient). Part of GSK £275M UK expansion. Primary world source for innovator-grade salbutamol API. Montrose, Angus, Scotland.

H&T Presspart Blackburn — Inhalation Product Technology Centre

GB

H&T Presspart · Lancashire, England · Manufacturing

Primary UK pMDI canister manufacturing and plasma coating facility. Houses the IPTC for low-GWP propellant development. Whitebirk Industrial Estate, Blackburn, Lancashire BB1 5RF.

Koura / Orbia Runcorn Pharmaceutical Propellant Plant

GB

Koura (Orbia Fluor & Energy Materials) · Cheshire, England · Manufacturing

World's largest integrated facility for pharmaceutical-grade HFC production. Manufactures Zephex 134a and 227ea. Adjacent HFA-152a facility opened March 30, 2022 — world's first commercial pharmaceutical-grade HFA-152a plant. The Heath Business & Technical Park, Runcorn WA7 4QX.

Meggle Wasserburg am Inn Pharmaceutical Excipients Plant

DE

Meggle Pharma · Bavaria · Manufacturing

Primary production site for MEGGLE InhaLac inhalation-grade lactose monohydrate. Specialized spray-drying and air-classification processes. Wasserburg am Inn, Bavaria, Germany.