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Syrup Manufacturing CDMO Companies
Oral Syrup Contract Manufacturing Services

Your Trusted Partners for Oral Syrup Contract Manufacturing and Development

Showing 18 facilities
Laboratorio REIG JOFRE, SA (TOLEDO PLANT)
Spain

Laboratorio REIG JOFRE, SA (TOLEDO PLANT)

LABORATORIO REIG JOFRE SA

Betalactam antibiotics (FDF) development and manufacturing state-of-the-art facilities.

MARKETS: DIGEMID (Peru), ANVISA (Brazil), ISP (Chile), Russian Health Authorities, EMA (EU), SFDA (Saudi Arabia), TGA (Australia), INVIMA (Colombia), MHRA (UK)

BATCH SIZE: Medium, Large

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS

COMPLIANCE: ISP (Chile BPM), Roszdravnadzor (Russia GMP), EMA (EU GMP), DIGEMID, UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), TGA (Australia GMP), SFDA (Saudi Food & Drug Authority), ECOVADIS, INVIMA, Health Canada (Canada GMP)

CONTROLLED SUBSTANCES: Lowest potential for abuse

REGION: Europe, APAC, LATAM, North America, MENA

USE: Human, Veterinary

SERVICES: Analytical / QC services, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day)

BSL (Biological Safety Level): 1

THERAPEUTIC AREAS OF EXPERTISE (ATC): (J) Antiinfectives for systemic use

Sidefarma
Portugal

Sidefarma

Sidefarma SA

CMO specialized in the manufacture of small and medium size batches for pharmaceutical companies across the world in regulated markets.

MARKETS: DIGEMID (Peru), Turkish Health Authorities, EDE (UAE), PMDA (Japan), EMA (EU), SFDA (Saudi Arabia), TGA (Australia), Health Canada (Canada), MHRA (UK)

BATCH SIZE: Small, Medium

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS

COMPLIANCE: EMA (EU GMP), UAE Ministry of Health & Prevention, ISO

CONTROLLED SUBSTANCES: Lowest potential for abuse, High potential for abuse & medical use, Lower potential for abuse, Low potential for abuse

REGION: Europe

USE: Human

SERVICES: Analytical / QC services, Manufacturing services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

FAES FARMA | DERIO facility
Spain

FAES FARMA | DERIO facility

FAES FARMA

Developer and manufacturer of human medicinal products.

MARKETS: DIGEMID (Peru), ANMAT (Argentina), EDE (UAE), ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), Russian Health Authorities, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

BATCH SIZE: Small, Medium, Large

THERAPEUTIC AREAS OF EXPERTISE (ATC): (R) Respiratory system, (M) Musculoskeletal system, (G) Genito urinary system and sex hormones, (J) Antiinfectives for systemic use, (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals, (N) Nervous system

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS

COMPLIANCE: ISP (Chile BPM), Roszdravnadzor (Russia GMP), ANMAT (Argentina nueva GMP), EMA (EU GMP), PMDA/MHLW (Japan GMP), DIGEMID, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), French Service-Public (CIR), TGA (Australia GMP), FDA (cGMP), NMPA (China GMP), ECOVADIS, ISO, INVIMA, Health Canada (Canada GMP), MSPAS, MFDS/KFDA (Republic of Korea GMP), COFEPRIS

REGION: Europe

USE: Human

SERVICES: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 1 / low-hazard (PDE > 10,000 µg/day)

Adragos Pharma |  Athens
Greece

Adragos Pharma | Athens

Adragos Pharma

Specializes in the development of Value Added Medicines and has been recently upgraded with HPAPI capabilities.

MARKETS: ANMAT (Argentina), EDE (UAE), ANVISA (Brazil), PMDA (Japan), FDA (USA), CDSCO (India), EMA (EU), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), MHRA (UK)

BATCH SIZE: Small, Medium, Large

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, SERVICES

COMPLIANCE: EMA (EU GMP), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), FDA (cGMP), NSF, NMPA (China GMP), ISO, MFDS/KFDA (Republic of Korea GMP)

CONTROLLED SUBSTANCES: Lowest potential for abuse, High potential for abuse & medical use, Lower potential for abuse, Low potential for abuse

REGION: Europe

USE: Human

SERVICES: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

Seda Pharma Development Services
United Kingdom

Seda Pharma Development Services

Seda Pharma Development Services Ltd

Seda Pharmaceutical Development Services specialises in integrated Pharmaceutical Development and Clinical Pharmacology.

MARKETS: DIGEMID (Peru), ANMAT (Argentina), Turkish Health Authorities, EDE (UAE), Rest of World, ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), CDSCO (India), Russian Health Authorities, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

BATCH SIZE: Small, Medium

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS

REGION: Europe

USE: Human

COMPLIANCE: MHRA (UK GMP), ECOVADIS

SERVICES: Analytical / QC services, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

THERAPEUTIC AREAS OF EXPERTISE (ATC): (M) Musculoskeletal system, (G) Genito urinary system and sex hormones, (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals, (N) Nervous system, (B) Blood and blood forming organs

PHARMALOOP S.L. - a Salvat Company
Spain

PHARMALOOP S.L. - a Salvat Company

Laboratorios Salvat

Fully integrated CDMO solutions for Blow-Fill-Seal (BFS), sterile multidose, non-sterile multi-dose, sachets, capsules and tablets.

BATCH SIZE: Small, Medium, Large

CATEGORY / PRODUCT: FDF / DRUG PRODUCTS, PARTICLE ENGINEERING

COMPLIANCE: EMA (EU GMP), FDA (cGMP), ISO

REGION: Europe

USE: Human

SERVICES: Analytical / QC services, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

MARKETS: FDA (USA), EMA (EU)

THERAPEUTIC AREAS OF EXPERTISE (ATC): (V01) Allergens, (S) Sensory organs

BSL (Biological Safety Level): 1

OEB (Occupational Exposure Banding): 1 / low-hazard (PDE > 10,000 µg/day)

Limited view

FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

Lannetts main manufacturing site sits in Seymour, Indiana, and includes capabilities for Oral Solid Dose (OSD) and Liquids.

Location available after registration

Limited view

FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

Israeli CDMO specialized in the development and GMP manufacturing of complex synthetic drug products and chemistry-based medical devices.

Location available after registration

Limited view

FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

We support drug development with small batch manufacturing services at all stages of the drug development process.

Location available after registration

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Oral syrups are a preferred dosage form for pediatric and geriatric populations due to their ease of swallowing, flexible dosing, and palatable taste. They’re also commonly used in OTC and nutraceutical products. To ensure stability, taste, and GMP compliance, pharmaceutical and consumer health brands turn to experienced syrup manufacturing CDMO companies.

With full-service oral syrup contract manufacturing, these CDMOs provide formulation development, flavor masking, sterile or clean filling, and scalable packaging options for global distribution.

How to Choose Syrup Manufacturing CDMO Companies

When selecting among syrup manufacturing CDMO companies, key factors include:

  • Expertise with sugar-based and sugar-free formulations
  • Experience with APIs, herbal extracts, vitamins, and minerals
  • Batch flexibility for clinical and commercial production
  • Viscosity control and homogenization capabilities
  • Taste masking and flavor development for pediatric products
  • Bottle filling with tamper-evident and child-resistant closures
  • Regulatory support for OTC, Rx, and nutraceutical products
  • Cold chain and light-sensitive ingredient handling, if needed

The ideal CDMO ensures the syrup is stable, palatable, and compliant with global standards.

Key Services Offered by Oral Syrup Contract Manufacturers

Top-tier oral syrup contract manufacturing providers typically offer:

  • Formulation and stability development
  • Sweetener and preservative system design
  • Flavor selection and masking technology
  • Viscous liquid blending and homogenization
  • GMP filling into bottles, unit-doses, or stick packs
  • Capping, labeling, and serialization
  • Stability and microbial testing under ICH conditions
  • Regulatory documentation for global submissions

These services cover everything from antitussive syrups to multivitamin tonics and pediatric formulations.

Advantages of Partnering with Syrup Manufacturing CDMO Companies

Working with expert syrup manufacturing CDMO companies offers key advantages:

  • Better patient compliance through taste-optimized, easy-to-swallow products
  • Fast development using syrup formulation platforms and ready-to-scale processes
  • Global packaging options for multiple markets
  • Support for sugar-free, alcohol-free, and clean-label trends
  • End-to-end project management from formulation to commercial supply

Syrups remain a go-to dosage form for chronic and OTC therapies — and the right CDMO ensures they meet patient and regulatory expectations.

Syrup Manufacturing CDMO Companies

Some of the most trusted syrup manufacturing CDMO companies include:

  • Lannett: Oral Solid Dose (OSD) and Liquids, including syrups. [See CDMO profile]
  • Pharmaloop (a Salvat company): Fully integrated CDMO solutions for Blow-Fill-Seal (BFS), sterile multidose, non-sterile multi-dose, syrups, sachets, oral solutions, and tablets. [See CDMO profile]
  • Reig Jofre: FDF development and manufacturing in state-of-the-art facilities. [See CDMO profile]
  • FAES FARMA: Developer and manufacturer of human medicinal products. [See CDMO profile]
  • I+Med: Developer and manufacturer of new drug products with controlled release technologies. [See CDMO profile]
  • Adragos Pharma: Specializes in Value Added Medicines, manufacturing oral liquids, syrups, semisolids, and oral solids (OSD). [See CDMO profile]
  • Sidefarma: Specialized in small- and medium-batch manufacturing for pharmaceutical companies, producing oral liquids, semisolids, syrups, and oral solids (OSD). [See CDMO profile]
  • Darnytsia Kyiv: Advanced facilities with strict quality control and expert staff, delivering compliant and innovative solutions. Manufacturing oral liquids, semisolids, syrups, and oral solids (OSD). [See CDMO profile]
  • Seda Pharma Development Services: Specialised in integrated Pharmaceutical Development and Clinical Pharmacology to facilitate the efficient development of optimal medicinal products, ranging from conventional to complex formulations, by leveraging scientific excellence. [See CDMO profile]

Related Information

Let MAI CDMO Help You Find the Right Syrup Manufacturing CDMO Partner

At MAI CDMO, we connect pharma and nutraceutical companies with experienced syrup manufacturing CDMO companies offering full-service oral syrup contract manufacturing. Whether you´re developing a pediatric syrup, launching a global multivitamin product, or scaling an herbal extract, we’ll help you find the right partner for your formulation, filling, and packaging needs.

Need a reliable partner for your syrup production? Contact us today and find your ideal CDMO match.