Pharmaceutical-grade Monk Fruit for Drug & Supplement Manufacturers

Applications Β· Pharmaceutical

Pharmaceutical-grade Monk Fruit
for Drug & Supplement Manufacturers

Monk fruit extracts serve as a natural, high-purity excipient for taste masking, palatability improvement and functional sweetening in oral pharmaceutical formulations, OTC products and nutritional supplements β€” where safety, traceability and documentation are non-negotiable.

GMP Manufactured Full Batch Traceability COA & TDS Available HACCP Certified Mettler-Toledo Metal Detection
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Pharmaceutical Use Cases β€” Extracts & Concentrates
Where monk fruit ingredients add value in drug and supplement manufacturing
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Traditional Chinese Medicine (TCM) Formulations
Added to herbal decoctions and TCM preparations as a co-ingredient to mask bitter herbal flavours and improve palatability. Enhances patient compliance without altering the therapeutic profile.
Flavour PowderV20Concentrate MFJC
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Oral Drug & Supplement Taste Masking
Masks bitterness in vitamins, minerals, APIs and herbal actives in liquid syrups, chewable tablets, and dissolvable strips. Creates a pleasant sweet note that improves patient β€” especially paediatric β€” acceptance.
V50V60V75
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Oral Liquid Preparations
Syrups, oral drops, and liquid supplements for diabetic or weight-conscious patients where sugar is contraindicated. Zero glycaemic impact enables use in glucose-sensitive formulations without reformulation risk.
V50Concentrate MFJQ
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Nutritional Supplements (Nutraceuticals)
Gummies, soft gels, chewable lozenges and effervescent tablets β€” monk fruit extract provides sweetness while keeping the formulation free from sugar, artificial sweeteners and calorie contribution.
V20V50V75
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Monk Fruit Juice Concentrate β€” Pharma & OTC Applications
The MFJC series is particularly suited to throat-soothing and respiratory OTC products
Product / OTC CategoryRecommended SeriesFunctional RoleKey Properties
Throat lozenges & cough drops MFJC Throat-soothing function + sweetening Rich monk fruit flavour, 15–20Γ— sweetness, anti-inflammatory properties
Cough syrup & lung supplements MFJCMFJF Taste masking + therapeutic support Soothes lungs, opens airway, complements herbal APIs
Tobacco & nicotine products MFJC Reduces combustion tar content Lowers tobacco oil content, natural additive for harm reduction
Paediatric oral medicines MFJQV50 Sugar-free taste improvement GRAS for infant foods Β· Zero sugar Β· No artificial additives
Diabetic OTC supplements V60V75 Zero-GI sweetening excipient No glycaemic impact Β· 0 kcal Β· Compatible with diabetic diet protocols
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Quality Assurance & Documentation
Pharmaceutical buyers require more than just a product β€” they need full documentation and traceability Β· View Extracts β†’  |  View Concentrates β†’
GMP Manufacturing
Both production bases operate under GMP standards. All processes comply with HACCP and ISO22000 food safety management systems.
Full Batch Traceability
From contracted farms through extraction and packaging β€” every batch is traceable. COA issued per batch with complete analytical data.
Solvent Purity
Only purified water and food-grade ethanol used in extraction. Zero industrial solvents. Critical for pharma-grade ingredient acceptance.
Metal Detection
Mettler-Toledo metal detectors plus magnetic grate filters on all production lines β€” pharmaceutical-standard contamination control.
Available Documents
COA (Certificate of Analysis), TDS (Technical Data Sheet), MSDS, allergen declaration, heavy metals testing, microbial test reports.
Automated Production
Fully automated, digitally controlled lines. Industry-exclusive 80m+ counter-current extraction line ensures batch consistency.
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Certifications Relevant to Pharma Buyers
GMP
Good Manufacturing Practice β€” both bases
HACCP
Hazard analysis critical control point certified
ISO 22000
Food safety management system
BRC
British Retail Consortium β€” EU/UK markets
USDA Organic
NOP certified β€” US pharma supply chains
Kosher KOF-K
Certified kosher excipient use
Halal ARA
JAKIM & BPJPH recognised
FSMA-FSVP
FDA food safety compliance for US import
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Why Pharma Manufacturers Choose SanLengBio
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Regulatory-ready Documentation
Full documentation package ready: COA, TDS, MSDS, allergen & heavy metal reports. Supports your regulatory submissions in US, EU, and Asia-Pacific.
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Pharma-compatible Purity
High-purity Mogroside V grades (50%–75%). No industrial solvents. Mettler-Toledo metal detection on all lines. Consistent batch-to-batch specification.
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Custom Specification Support
R&D team collaborates on excipient specifications. Custom particle size, sweetness ratio, and blend formulations available for OEM pharma clients.
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Multi-regional Compliance
GRAS (US FDA), approved in Australia, NZ, Japan. BRC and ISO22000 for EU. Halal and Kosher for Middle East and global Muslim/Jewish market pharma.
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Stable Supply Assurance
300-tonne daily capacity. 33+ years of monk fruit expertise. Contracted farms with government-backed demonstration base ensure raw material security.
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Technical & Regulatory Support
Dedicated account support for pharma buyers. Assistance with supplier qualification audits, documentation requests, and application development.

Qualifying a new excipient supplier?

Request a full documentation package (COA, TDS, MSDS) or arrange a supplier qualification audit.

Request Documentation β†’

Factory Price With High Quality Product

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