Aptargroup, Inc.NYSE: ATR

Bank of America 2026 Injectable Drug Packaging Virtual Field Trip

· Issued by Aptargroup, Inc.


Gael Touya

President, Aptar Pharma

Sai Shankar

President, Aptar Pharma M&A, Strategy, Business Development

Mary Skafidas

SVP, Investor Relations & Communications

Bank of America Injectable Drug Packaging Virtual Field Trip

March 2, 2026

1



Global Leader in Drug Delivery, Dosing and Protection Technologies, and Consumer Product Dispensing

2025 % of Total Reported Sales



Beverage 5%

2025 Adjusted EBITDA3,4

Home Care 3%

Personal Care 16%

Food 10%

Closures 19%

$3.8B1

Beauty 35%

Pharma 46%

Proprietary Drug Delivery Systems2

Closures

13%

Beauty

18%

$815M

Pharma

69%

33%

Fragrance, Facial Skincare and Color Cosmetics

20%

Injectables 8%

Active Material Science Solutions 5%

1: 2025 Annual Revenue

2: Proprietary Drug Delivery Devices includes Prescription, Consumer Healthcare and Digital Health Markets

3: See "Forward-Looking Statements and Non-GAAP Financial Measures" slide for definitions and Appendix for GAAP reconciliation

4: Segment percentages calculated as the percentage of Adjusted EBITDA for Reportable Segments

3

Technologies and Industrial Capabilities Deployed Across End Markets

In Place

Developing

Proprietary Technology Platforms1

Industrial Capabilities

Dispensing Fine Mist Pumps Dispensing Closures Dispensing Lotion Pumps Active Materials



Elastomeric Components Airless Systems

Aerosol Valves & Bag-On-Valves Services

Digital + Connected Devices Precision Injection Molding High Speed Assembly, AI QC2 Metal Stamping & Anodizing Decoration

Pharma Beauty Personal Care Home Care Beverage Food

Sustainable Solutions

Industry Leading Innovation, Unmatched Reliability

Closures

16%

22%

7,300+

Patents (granted or pending)

62%

Consistent Patent Investments1

Beauty

Pharma

Our advanced dispensing and dosing solutions are intended to maximize user satisfaction, delivering superior value to both customers and end users.

R&D spend as a percentage of sales for Aptar is ~3%3 with a larger portion of the R&D spend going to Pharma

  • Proprietary Intellectual Property

    Aptar designs and owns its IP

  • Pharmaceutical Excellence

    Aptar meets ISO 5, 6, 7, 8, and 9 cleanroom standards, with clean rooms in every facility to help ensure product integrity and safety

  • Regulatory Expertise and High Reliability

    Aptar supports emergency medicines with demonstrated reliability of 99.999%2. Regulatory know-how makes us a key partner, accelerating success from strategy to commercialization

  • Advanced Dispensing Solutions

    Aptar's proprietary technologies deliver high-performance dispensing, enhancing patient and consumer experiences

  • Innovation & Rapid Development

    Integrated labs and prototyping accelerate efficient solution design

  • Human Factors Expertise

    We embed human factors into design to help ensure safety, usability, and a superior user experience

    1: Granted and pending as of April 2025 based on company research and publicly available information

    2. As demonstrated in NDA filings using our dispensing systems for emergency situations 3: For fiscal year 2025.

    5

    Well-Positioned for Long-Term Revenue Growth

    Beauty

    $38B

    Pharma

    $165B

    Closures

    $7B

Closures

~2%

Beauty

~4%

Pharma

~7%

  • Aptar plays in large and growing TAMs

  • Projections for market growth support long-term revenue growth

  • Focused execution and driving the right investment mix expected to drive revenue growth at or above the market

  • Highly diversified model, with no single product or geography driving long-term growth

Total Addressable Market Across Aptar's Growing End Markets1

Long-Term Market Projected Growth Rates



Recent Recognitions

Our award-winning commitment to sustainability is a competitive advantage that drives impact for our customers

CDP

Climate A List

Newsweek

In the Top 100

America's Most Responsible

Forbes

One of the

World's Top Companies For

TIME

One of the

World's Most Sustainable

EcoVadis

Sustainability Rating

Platinum

Top 1%

Barron's*

In the Top 100

Most Sustainable Companies

ISS ESG



Achieved

Prime Status

USA Today

One of

America's Climate Leaders

2024-2025

Companies

Women

Companies

2021 - 2025

from 2019-2025

from 2020-2024

2023-2025

2020-2026

from 2021-2025

2024-2025

*Used with permission. ©2025 Dow Jones & Company, Inc.

7

Aptar Pharma

Aptar Pharma - At a Glance

FY 2025 % of Pharma Segment Sales

Active Material Science Solutions

10%

Injectable Solutions

& Components

Proprietary Drug

Delivery Systems1

19%

$1.7B

in Revenue

71%

We are a proprietary leader in precision drug dosing and dispensing active in highly regulated markets

  • IP Breadth

  • Diversified Portfolio

  • Conversion: Originator → Generic Transition → OTC

  • Regulatory expertise makes us a trusted partner

  • Our services help enable early engagement

  • Our digital health offerings set us apart from other suppliers

  • A strong balance sheet supports pharma investment and long-term strength

FY 2025











Core Sales Growth %2 3%











Adjusted EBITDA Margin %2 35.0%







% of Total Revenue 46%



% of Total Adjusted EBITDA2 69%

1: Proprietary Drug Delivery Devices includes Prescription, Consumer Healthcare and Digital health Markets.

Strong Market Position Fortified by Differentiated Position

Aptar Pharma's Strengths

Increasing Regulatory Complexity

Proven track record in supporting approval of combination products (molecule + delivery system) in US and EU. Our experts work collaboratively with regulatory agencies to address new product specific guidance.

Significant Engineering & Scientific Know-How

Strong IP Portfolio, bolstered by decades of expertise. Our scientific affairs teams are building an understanding of pathway modeling.

Quality & Reliability

Proven reliability. Multiple market references with a proven regulatory track record.

Long-Standing Customer and Partner Relationships

30+ years of experience. Established lines eliminates capacity reservation.

Capital Intensity

Global footprint -- Significant investment in manufacturing capacity has improved our ability to meet customer needs and market demands.

Total Drug Sales by Delivery Route

Dermal / Transdermal

Well positioned with proprietary products Technology platform shared with Beauty segment

Respiratory

2%

Eye Care

Well positioned with proprietary products

Other Routes







Well positioned with proprietary products

5% 4%

1%



43%

$1.7T

Total Drug Sales Market1

45%

Oral

Strong growth potential

Focused on specialized high-value market for drugs with sensitive formulations





Injectables

Growing position with expanded capacity in

High-Value Product offerings

Aptar Pharma: Global Reach, Trusted Partner, Broad Offerings

$2,000

Reported Net Sales

(in Millions $)

$700

Adjusted EBITDA

(in Millions $)

$1,800

$1,600

$1,400

$600



$500

$1,200

$1,000

$800

$400

$300

$600

$400

$200

$-



2016 2017 2018 2019 2020 2021 2022 2023 2024 2025

$200

$100

$-

2016 2017 2018 2019 2020 2021 2022 2023 2024 2025

FY 2025

Net Sales

Reported Net Sales Growth % Adjusted EBITDA1

Adjusted EBITDA Margin %1

$1.7B

6%

$608M 35.0%

1: See Appendix for definitions.

12



Prescription Drug Therapeutic Areas

For Respiratory, Injectable, Ophthalmic, and Dermal Drug Delivery Routes

Top Therapeutic Areas by Average Weighted Value of Opportunities in Pipeline

(As of September 30, 2025)

  1. Respiratory

  2. Biologics (Inj.)

  3. Systemic Nasal Drug Delivery

    o Central nervous system (CNS), Pain management, Emergency medicine

  4. Small Molecule (Inj.)

  5. Ophthalmology

  6. Allergic Rhinitis

  7. Vaccines (Inj. and Nasal)

  8. Dermatology

Key Takeaways

  • Diverse therapeutic areas support a well-diversified portfolio

  • Injectables have taken an increasingly prominent role in the pipeline

  • As systemic nasal drug delivery expanded, nasally delivered CNS therapies represented the majority of opportunities

  • Historically, the pipeline contributes about 10% of annual revenue, while 90% is driven by repeat business*

    Our core business continues to deliver-systemic nasal delivery is accelerating, and Injectables now accounts for a greater portion of the pipeline

  • Pharma's primary growth driver has been volume growth and favorable mix shift within repeat business

    Deep-dive of Proprietary Drug Delivery Systems Pipeline



    Metabolism

    Obesity Diabetes

    Musculoskeletal

    Muscular Dystrophy Creatine Deficiency ALS

    Vaccine & Antiviral

    COVID-19 RSV

    Influenza Universal Flu mAbs / mRNA

    Cardiovascular

    Molecules

    Neurological Disorders

    Autism Spectrum Sleep Disorders Prader-Willi

    Neurodegeneration

    Alzheimer's Dementia Parkinson's Huntington Multiple Sclerosis

    Aging

    Eye Diseases

    Dry Eye Glaucoma

    Mental Health

    Stroke / Heart Failure Cardiac Arrhythmia

    Edema and Tachycardia (Just Approved)

    ADHD

    PTSD / Anxiety Schizophrenia

    Depression Addiction

    Bipolar Disorders

    Oncology

    Glioblastoma Breast Cancer Brain Cancer Meningioma

    Traumatic Injury

    Traumatic Brain Injury Newborn Brain Damage Spinal Cord Injury

    Lifecycle of a Nasally Delivered Molecule Using Aptar's Proprietary Drug Delivery System

    Development

    1988

    Originator

    1994

    Generics

    2006

    Brand Extension 2007

    Originator Goes

    OTC Status

    2014

    Generics Go

    OTC

    2017

    Drug X first approved for prescription in 1994 with Aptar's nasal delivery system (1st generation) in its Drug Master File (DMF)

  • Using Aptar's Delivery technology remains the delivery system (with improvements, IP, etc.) throughout the lifecycle of the drug

  • More than 3 billion Aptar delivery systems have been sold for this molecule

  • Aptar has received revenue for its respective delivery systems for this molecule for 30 years and counting

Revenue from Drug X

30x

in revenue

One molecule can create sustained revenue

Pipeline launches add to steady stream of revenue from growing repeat business1

1995

1996

1997

1998

1999

2000

2001

2002

2003

2004

2005

2006

2007

2008

2009

2010

2011

2012

2013

2014

2015

2016

2017

2018

2019

2020

2021

2022

2023

2024

Originator Generic OTC

Added Early-Stage and Late-Stage Capabilities to Bolster Core Business

Discovery

Clinical Trial Development

Market Launch and LCM

Discovery and

Pre-Clinical

From Phase I to Phase III

Commercial

Phase IV and LCM

Services support, accelerate and derisk our customers' product development and enhance patients' experiences

From NDAs to ANDAs and 505b2 filings, our regulatory expertise and

Historical positioning

credibility help derisk pharma company's submissions by leveraging 30+

years of experience supporting our customers and responding to regulators

API

Device C

Formulation

Patient

Insight

Analytical

testing

Human

Factors

Clinical

supplies

Regulatory

support

Clinical

Manufacturing

Commercial

Manufacturing C Release

Patient

onboarding

Device supply-patient

monitoring solutions

Design

fo

rmulation d

Device G

ev.

Clinical trials

Regulatory fillings

Manufacturing

Market launch G post-launch

Adding Value Throughout the Drug Development Process

Proprietary Drug Delivery Systems (PDDS)

From Prescription to OTC

FY 2025 % of Pharma Segment Sales



Active Material Science Solutions

Injectable Solutions and Components

71%

Proprietary Drug Delivery Systems1

Prescription2 - 51% Consumer Healthcare - 20%



Application Fields

  • Allergy

  • Pulmonary

  • Systemic Nasal Drug Delivery

  • Cough and Cold

  • Dermal

  • Eye Care

  • Vaccines and Antivirals

  • Analgesics

  • Digestives

- Pain, CNS and Emergency Meds

1: Proprietary Drug Delivery Devices includes Prescription, Consumer Healthcare and Digital health Markets. 2: Prescription includes the Digital Health Market.

Nose-to-Brain

NextGen Propellants

Biologics / Powders / Vaccines

Building Blocks for Growth for PDDS

Growing Applications for PDDS

Nose-to-Brain

Emergency Medicine

/ CNS / Pain Management

Eye Care

Local Delivery Targeting Inflammation



Emergency Medicine / CNS / Pain Management

Eye Care

Application Fields for PDDS Continue to Expand

Emergency Medicine / CNS / Pain Management

Eye Care

Allergy Asthma/COPD Dermal Drug Delivery Migraine

Nasal Saline Nasal Decongestion

Allergy Asthma/COPD Dermal Drug Delivery Migraine

Nasal Saline Nasal Decongestion

Allergy Asthma/COPD Dermal Drug Delivery Migraine

Nasal Saline Nasal Decongestion

Past

(Commercial Launches)

Present

(Commercial Launches)

Future

(Commercial Launches)

Therapeutic areas that use our delivery systems in nasal, inhalation, ophthalmic and dermal continue to expand



Nose-to-Brain Drug Delivery Fueling Our Long-Term Growth
  • Nasal mucosa offers an alternative pathway to the brain that bypasses the Blood Brain Barrier with targeted delivery to site of action

  • Potential to open new therapeutic areas and new molecules to nasal administration

  • Highly attractive therapeutic areas fall within this pathway

    - Neurodegenerative diseases or Psychiatric conditions e.g.

    Alzheimer's, Parkinson's, depression

  • Biologics and complex molecules are showing early promising results with antivirals, monoclonal antibodies, and peptides (GLP-1s)

    Nasal delivery can be used for almost any sized molecule It's not just for small molecules anymore

  • We've partnered with Wake Forest School of Medicine on a groundbreaking study confirming that intranasal insulin-delivered through a one of our proprietary nasal drug delivery systems -safely reaches 11 critical brain regions tied to memory in older adults

Drug Formulation

Cerebrum

Olfactory Bulb

Olfactory Nerves

Brain Stem

Trigeminal Nerves

Competitive Differentiator

Device &

Formulation Dev.

Clinical

Trials

Regulatory

Filings

Market

Launch & Post-Launch



Our Robust Drug Master File (DMF) Submission Services Support Our Customer's Regulatory Filings

DMF

File Investigational New Drug Application (IND)

Customer references the Master File

File New Drug Application (NDA)

Our proprietary technology is reflected in regulatory documentation, including Drug Master Files referenced in our customers' regulatory filings, with ongoing regulatory support as products progress through regulatory and commercial stages

Our nasal delivery technology has a proven track record of reliability

Applicants must demonstrate that the device can meet a reliability target of 99.999% with a 95% level of confidence or a 1:100,000 failure frequency

We have demonstrated this capability with real-world evidence in approved and commercialized applications

1

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