PQQCapsule Contract Manufacturing and Private Label Customization
PQQ is commonly used in dietary supplements for cognitive support, sports nutrition, and anti-aging. We offer a complete contract manufacturing service—from raw material evaluation and custom formulation to full-scale production.
4 types
Available dosage forms for contract manufacturing
10-40mg
Common Specifications
3-7 days
Sample Lead Time
45-60 days
Standard Lead Time
AboutPQQ（Pyrroloquinoline Quinone）
PQQ (pyrroloquinoline quinone) is a quinone compound typically supplied as disodium pyrroloquinoline quininate in dietary supplement ingredients, commonly available in capsules, tablets, and powder stick packs.
In OEM formulations, PQQ is commonly combined with coenzyme Q0, NMN, ergothioneine, and spermidine to create synergistic blends targeting energy metabolism, antioxidant support, or cellular maintenance.
PQQ's regulatory status, permitted uses, and limits vary by market. Confirm compliance with target market regulations before finalizing the formula and label.
Key OEM Metrics
- Manufacturing Formats4Types; specifications customized based on brand positioning
- Sample lead time: 3-10 business days; Mass production standard cycle: 45-60 days
- Produced in a GMP, ISO 22000, and HACCP certified facility
- Batch COA; third-party testing available upon request.
PQQAvailable Dosage Forms and Specifications
The table below shows common configurations. Actual content, capsules per bottle, and packaging format can be adjusted according to brand requirements.
| Dosage Form | Common Specifications | Minimum Order Quantity |
|---|---|---|
| Hard Capsules | 10 / 20 / 40 mg per capsule, 60-120 capsules per bottle | 18 thousand grains |
| Softgel | 10 / 20 mg per capsule, oil-based suspension process | 30 thousand grains |
| Tablet | 10 / 20 mg per tablet, film-coated | 18 million pieces |
| Striped Powder | 10 / 20 mg per dose; can be mixed with granules | 10 thousand records |
Hard Capsules
Specifications:10 / 20 / 40 mg per capsule, 60-120 capsules per bottle
Minimum Order Quantity:18 thousand grains
Softgel
Specifications:10 / 20 mg per capsule, oil-based suspension process
Minimum Order Quantity:30 thousand grains
Tablet
Specifications:10 / 20 mg per tablet, film-coated
Minimum Order Quantity:18 million pieces
Striped Powder
Specifications:10 / 20 mg per stick; may be combined with other supplements
Minimum Order Quantity:10 thousand records
PQQCompound Formula Direction
Common blending approaches are listed below. Final ratios and processes are determined by the R&D team based on stability test results.
Energy Metabolism Bundle
PQQ + CoQ100
Classic mitochondrial energy formula tailored for daily nutrition in mature adults.
NAD+ Dual-Pathway Combination
PQQ + NMN
For anti-aging formulations targeting cross-border channels, first verify the regulatory status of ingredients in the target market.
Antioxidant Network Blend
PQQ + Ergothioneine + Vitamin C
Ideal for daily antioxidant use, balancing formula stability and cost.
Cell Care Kit
PQQ + Spermidine
For high-end anti-aging formulations, evaluate blend ratios and process feasibility.
PQQOEM Process
Complete the journey from requirements to delivery in five steps, with written confirmation at every key milestone to prevent batch deviations.
- 01
Requirement Assessment
Confirm dosage form, strength, target market, packaging format, and estimated first-order volume to generate a feasibility assessment.
- 02
Formula Sampling
The R&D team will adjust the formulation and process based on positioning, delivering samples along with initial taste and appearance feedback within 3-7 working days.
- 03
Compliance & Labels
Verify the ingredient list, nutrition label, and claim wording against the permitted status of ingredients in the target market before production.
- 04
Mass Production
Raw material inspection, batching, production, primary packaging, and secondary packaging. Full-process sampling with records of key process parameters.
- 05
Quality Inspection Delivery
Issue COA, arrange third-party testing as needed, and proceed with outbound logistics upon confirming batch consistency.
Compliance Essentials and Quality Control Guidelines
Raw material identity, claim wording, and test items are the most common pain points in OEM projects. Verify each one before production starts.
- Ingredient Identity: PQQ is regulated as either a novel food ingredient or a dietary supplement ingredient depending on the market. Before production, verify the approved scope, limits, and labeling requirements for your target market.
- Labeling: Do not use claims related to disease treatment, cure, or drug substitution. All efficacy-related statements must comply with advertising and labeling regulations in the target market.
- Production Credentials: Our manufacturing facilities are certified under GMP, ISO 22000, HACCP, and other management systems. Certificates and system documentation are available upon request.
- Batch Testing: COA provided for each batch; third-party testing for heavy metals, microorganisms, and active ingredient content can be arranged per customer request.
- Confidential Formulation: Client-exclusive formulas and packaging designs are archived separately under a non-disclosure agreement and not used for other client projects.
This page provides OEM solutions and technical specifications. It does not constitute product efficacy claims or medical advice. Specific formulations, ingredient identities, labeling, and claims must comply with target market regulations and are subject to the final approved sample and contract agreed upon by both parties.
PQQFrequently Asked Questions for OEM Services
What is the minimum order quantity for PQQ capsule contract manufacturing?
Hard capsules: 18k units minimum; Soft capsules: 30k units minimum; Tablets: 18k units minimum. Small-batch sampling available during the prototyping phase; mass production costs are calculated based on dosage form and packaging type.
What dosage forms can PQQ be formulated into?
Supports hard capsules, soft capsules, tablets, and sachet powders. Common strengths are 10mg, 20mg, and 40mg, adjustable based on formulation requirements.
How long does it take from sampling to delivery?
Sample production: 3-7 working days. After formula and packaging confirmation, the standard lead time is 45-60 days, including raw material sourcing, manufacturing, quality inspection, and packaging.
Does it support custom blending?
Supported. Can be combined with ingredients such as Coenzyme Q10, NMN, Ergothioneine, and Spermidine. Our R&D team will first evaluate compatibility, stability, and process feasibility before providing samples.
Related Pages & Solutions
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View DetailsNeedPQQOEM Quote?
Please provide the dosage form, specifications, and estimated first-order quantity. We will respond with a feasibility assessment and price range within 1 business days.
Get Your Exclusive QuoteStandards & Authoritative References
NIH National Center for Biotechnology Information· Research on PQQ and Mitochondrial Biogenesis
U.S. Food and Drug Administration· Good Manufacturing Practices for Dietary Supplements
International Organization for Standardization· Explanation of the Food Safety Management System Standard
* All sources cited above are publicly available information from authoritative institutions and are for reference only.