30+ Years of Nutraceutical Manufacturing cGMP 21 CFR 111 · NSF Registered GMP
Hauppauge, New York, USA (631) 951-4908
Turn-Key U.S. Manufacturing

Nutritional Supplements Manufacturer

Premier contract manufacturing for dietary supplements, vitamins, and health formulas under strict cGMP and NSF controls for global buyers.

Proven B2B Partner

High-Quality Nutritional Supplement Manufacturing for Global Brands

Implementing premium nutrition into global consumer markets requires a reliable, compliant, and highly experienced manufacturing partner. At Bactolac Pharmaceutical, we provide cost-effective, high-capacity contract manufacturing for private label and custom dietary supplement formulations.

Operating from our 200,000+ square foot facility in New York, USA, we handle every stage of supplement production in-house — from raw material quarantine and custom formulation to automated encapsulation, high-speed tableting, analytical testing, and export packaging.

  • Full compliance with FDA 21 CFR Part 111 cGMP and NSF GMP registration
  • Advanced analytical & microbiological laboratories for batch verification
  • Scalable production capacity for emerging startups to global enterprise distributors
Finished powder, capsule, and tablet dietary supplements manufactured by Bactolac Pharmaceutical
Full Delivery Formats

Comprehensive Contract Manufacturing Capabilities

We work with brand owners, importers, and distributors across North America, Europe, Asia, and the Middle East to formulate and manufacture market-ready nutritional supplements.

Powder Blending

Custom Powder Blends

High-shear blending for protein powders, hydration formulas, sports nutrition drink mixes, collagen, and organic greens. Custom flavor profiling and stick-pack or tub packaging.

Encapsulation

Hard Shell & Softgel Capsules

Vegetarian, gelatin, and liquid-filled hard capsules available in sizes 000 to 4. Advanced options including delayed-release, nanoparticle, and enteric-coated capsules.

Compression

Tablets & Sublinguals

High-speed tablet compression including chewable, bi-layer, sublingual, time-release, and effervescent formulations finished with pharmaceutical glaze or custom color coatings.

Quality Compliance

NSF & NPA Certified

Our operations comply with NSF International and Natural Products Association standards, ensuring stringent raw material identity testing and batch purity monitoring.

Certified Standards

Kosher & Halal Available

We accommodate diverse market requirements with certified Kosher and Halal production capabilities, ensuring compliance with international religious dietary standards.

Turn-Key Packaging

Primary & Secondary Packaging

Complete filling and packaging services including wide-mouth jars, bottles, blister packs, gusset bags, stick packs, single-serve pouches, and custom outer cartons.

Laboratory technician conducting raw material identity testing
E-E-A-T Quality Assurance

Analytical & Microbiological Laboratory Controls

To meet global regulatory standards and retail marketplace requirements (including Amazon dietary supplement testing standards), our in-house quality control labs rigorously verify every lot before shipment.

  • Raw Material Authentication: Identity testing and heavy metal screening on 100% of incoming ingredients.
  • Potency & Composition Assays: Verifying exact active ingredient concentrations against batch formulas.
  • Microbiological Screening: Testing for pathogens, yeast, mold, and total aerobic plate counts.
  • Batch Documentation: Issuance of comprehensive Certificates of Analysis (COA) for seamless international customs clearance.
Competitive Advantage

Why Overseas Buyers Partner With Bactolac Pharmaceutical

30+ years of operational experience guarantees high production efficiency, tight quality controls, and reliable delivery timelines for cross-border trade.

Rapid Turnaround

Optimized supply chain management and automated equipment ensure fast lead times to bring products to market quickly.

Extensive Raw Inventory

Direct relationships with qualified worldwide ingredient vendors ensure reliable supply chains and consistent raw material availability.

High-Tech Facilities

State-of-the-art climate-controlled cleanrooms, segregated allergen lines, and automated packaging systems built for mass production.

Export Documentation

Complete support with Certificates of Free Sale, allergen declarations, BSE/TSE statements, and international regulatory documentation.

Knowledge Base

Frequently Asked Questions

Answers to common queries from international B2B purchasers and brand owners evaluating our manufacturing services.

Our state-of-the-art facilities operate strictly under FDA 21 CFR Part 111 cGMP guidelines and hold NSF International GMP registration. Additionally, we hold certifications with Quality Assurance International (QAI) for USDA Organic manufacturing, the Natural Products Association (NPA), Health Canada NHPD compliance, as well as Kosher and Halal production capabilities.

Yes. As active members of the Natural Products Association and QAI Organic certified facility operators, we adhere strictly to the USDA National Organic Program standards. We assist with clean-label ingredient sourcing, allergen-free processing, and certified organic formula validation.

Our qualified formulation scientists and analytical chemists work directly with your brand to create custom formulas or optimize existing formulations. Every batch undergoes rigorous identity, purity, potency, and microbiological testing in our two in-house QC laboratories before product release.

We provide complete export documentation packages including Certificates of Analysis (COA), Certificates of Free Sale, allergen declarations, BSE/TSE statements, heavy metal test reports, and batch production records tailored to regional regulatory authorities worldwide.

Start Your Supplement Manufacturing Project Today

Contact our technical engineering and customer management teams for feasibility analysis, custom formulation support, and production pricing.

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