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

Tablet Manufacturing

Custom dietary supplement tablet contract manufacturing — bi-layer, chewables, sublinguals, film-coated, and enteric-coated formulations scaled for global distribution.

Premier Contract Manufacturing

High-Speed cGMP Tablet Manufacturing for Global Brands

When expanding your brand into international retail channels or online marketplaces, product quality, dosage accuracy, and regulatory compliance are non-negotiable. At Bactolac Pharmaceutical, Inc., we specialize in high-capacity contract tablet manufacturing, producing premium dietary supplements that meet rigorous global standards.

Operating from our 200,000+ sq. ft. cGMP-certified facility in New York, USA, our expert formulation scientists and analytical lab technicians oversee every phase of production. From raw material milling and high-shear granulation to precision compression and specialized coating, we maintain complete control under one roof to deliver consistent, market-ready tablet solutions.

  • Full-service OEM/ODM custom tablet formulation and bench scale-up
  • In-house analytical and microbiological quality control testing
  • Comprehensive export documentation for international regulatory compliance
  • Advanced coating technologies: film, enteric, modified-release, and pharmaceutical glaze
High Quality Dietary Supplement Tablets Manufactured by Bactolac
Versatile Dosage Technologies

Comprehensive Custom Tablet Manufacturing Capabilities

Our automated high-speed tablet presses accommodate diverse shapes, sizes, colors, and functional delivery systems tailored to your brand's specific consumer needs.

Dual-Release Delivery

Bi-Layer Tablets

Separate incompatible ingredients or combine immediate-release and extended-release layers into a single dual-color tablet format for enhanced bioavailability.

Palatable Formulations

Chewable Tablets

Formulated with custom natural flavors, organoleptic masking, and optimized texture—ideal for multivitamins, kids' nutrition, and stomach-friendly mineral applications.

Rapid Absorption

Sublingual Tablets

Fast-dissolving sublingual tablets engineered for direct mucosal absorption, perfect for Vitamin B12, melatonin, and targeted botanical actives.

Targeted Release

Enteric-Coated Tablets

Specialized pH-sensitive polymer coatings protect sensitive enzymes, probiotics, or botanicals from acid degradation while preventing gastric discomfort.

Sustained Delivery

Time-Release & Extended-Release

Hydrophilic matrix technology controls ingredient dissolution over extended hours, ensuring stable, steady nutrient absorption throughout the day.

Hydration & Refreshment

Effervescent Tablets

Precision-engineered effervescent formulas for rapid dissolution in water, delivering instant drinkable electrolytes, vitamin C, and energy blends.

Advanced Tablet Compression Machine in cGMP Plant
Quality Assurance & Compliance

End-to-End Quality Control & Analytical Verification

Substandard manufacturing leads to batch rejection, weight variation, and friability issues. Our strict compliance under FDA 21 CFR Part 111 cGMP regulations ensures every tablet lot produced achieves verified potency, purity, and physical stability.

  • Raw Material Identity Verification: Quarantine and FTIR/HPLC identity testing on all incoming active raw materials and excipients.
  • In-Process Control (IPC): Continuous automated monitoring of tablet weight, thickness, hardness, friability, and disintegration times.
  • Aqueous & Organic Coating: Color-matching film coatings and moisture-protective seals using safe, non-toxic, clean-label materials.
  • Finished Batch Release: Microbe screening, heavy metal ICP-MS testing, and assay validation performed in our on-site laboratories.
Export Ready Solutions

Turn-Key Services Tailored for Overseas Importers

Bactolac Pharmaceutical serves brand owners, distributors, and pharmaceutical importers across North America, Europe, Asia, the Middle East, and Latin America. We understand the complex international trade standards required for seamless entry into your target market.

Our dedicated regulatory support team assists with compliant label artwork formatting, ingredient allowance checks, and standardized export documentation packages needed by foreign customs agencies.

  • Complete documentation: Certificate of Analysis (CoA), Certificate of Free Sale, allergen declarations, and BSE/TSE statements
  • Master Batch Record (MBR) and full lot traceability for institutional audits
  • Primary packaging options: HDPE bottles, glass bottles, wide-mouth jars, and blister packaging
  • Secondary packaging: Custom printed folding cartons, display boxes, and shipping containers
Turn-Key Dietary Supplement Packaging and Labeling
Audited Standards

Independently Certified & Registered Facility

Our facility holds recognized certifications ensuring compliance with U.S. federal guidelines and voluntary quality management standard programs.

NSF registered GMP certification mark
NSF contents certified program mark
Good Manufacturing Practice compliance certification
Quality assurance certification badge
Organic certification for supplement manufacturing
Natural Products Association member logo
Third-party audited manufacturing certification seal
Structured Execution

5-Step Contract Tablet Production Workflow

A transparent, milestone-driven development process from formula refinement to container shipment.

  1. Formula Review

    Collaborative consultation on actives, target dosage, excipient flowability, and market registration targets.

  2. Lab Pilot & Sample

    R&D benchtop batching, hardness checks, disintegration testing, and sensory taste sign-off for chewables.

  3. Blending & Granulation

    Quarantined ingredient weighing, fluid-bed or wet/dry granulation, and high-shear blend uniformity checks.

  4. Compression & Coating

    High-speed rotary press compression followed by protective aqueous film coating or enteric sealing.

  5. QC Testing & Packaging

    On-site lab assay clearance, bottle or blister filling, packaging, labeling, and export dossier release.

Contract Sourcing FAQ

Frequently Asked Questions: Tablet Manufacturing

Direct technical answers for commercial sourcing teams, distributors, and brand founders.

We formulate and manufacture bi-layer, chewable, sublingual, effervescent, time-release, enteric-coated, and film-coated tablets. Our team assists with custom shapes, sizes, break-lines, and organoleptic flavor profiles tailored to your brand strategy.

Production MOQs generally start around 25,000 to 50,000 finished bottled units or bulk powder/granulation equivalent. Pilot launch volumes can be evaluated based on raw material availability and specific tooling requirements.

Yes. We routinely prepare comprehensive international export packages including Certificates of Analysis (CoA), Certificates of Free Sale, allergen declarations, non-GMO statements, BSE/TSE declarations, and manufacturing flow diagrams for international customs clearance.

Our technicians perform strict in-process control testing at regular intervals during tablet compression. We measure tablet weight variation, thickness, hardness, friability, and disintegration rates to ensure every batch aligns strictly with master specifications.

We offer automated packaging in HDPE and PET bottles, glass jars, blister packs, unit-dose pouches, and gusset bags with tamper-evident induction seals, cotton fillers, and child-resistant closures.

Partner with a Trusted USA Tablet Manufacturer

Discuss your tablet formulation, target market requirements, and batch size with our technical project managers today.

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