30+ Years of Nutraceutical Manufacturing cGMP 21 CFR 111 · NSF Registered GMP
Hauppauge, New York, USA (631) 951-4908
Bactolac Pharmaceutical Contract Manufacturing Plant
Fast 48-Hour RFQ Turnaround

Request A Quote

Partner with an audit-ready U.S. cGMP contract manufacturer for capsules, tablets, powders, and custom formulations.

Direct B2B Quotations

Turnkey Contract Manufacturing Quotes for Global Brands

At Bactolac Pharmaceutical, we streamline the procurement process for international buyers, brand owners, and global distributors seeking premium dietary supplement manufacturing in the United States. Operating out of our 200,000+ sq. ft. cGMP-certified facility in New York, we handle every stage of production under one roof.

Whether you require custom formulation development, pilot batch scaling, or high-speed commercial production runs, our scientific and regulatory teams provide transparent unit pricing and comprehensive technical evaluations within 24 to 48 hours.

  • cGMP 21 CFR Part 111 compliant & NSF Registered manufacturing
  • In-house analytical & microbiological laboratory verification
  • Turnkey packaging, labeling, and cross-border export documentation
Supplement finished products manufacturing including capsules, tablets and powders
Procurement Requirements

Information Required for an Accurate Quotation

To provide a binding price quotation and clear delivery schedule, our formulation scientists and commercial estimators review key product parameters.

01. Dosage Form

Delivery Format

Specify two-piece hard capsules, softgels, bi-layer/chewable tablets, or high-dispersion powders.

02. Master Formula

Active Ingredients

Submit target ingredient potency, standardized botanical extracts, amino acids, or specialized actives.

03. Order Volume

Batch Quantities

Minimum production runs start at 25,000 bottle units for solids and 1,000 kg for bulk powders.

04. Packaging

Bottles & Pouches

Select wide-mouth HDPE/PET bottles, blister cards, stick packs, single-serve sachets, or gusset bags.

Quality Assurance Specialist conducting testing in laboratory
International Trade Ready

Export Compliance & Certificate Support for Importers

Navigating global customs regulations requires flawless batch documentation. Bactolac routinely provides complete regulatory compliance packages to support smooth customs clearance across Europe, Asia, Australia, the Middle East, and Latin America.

  • Certificate of Analysis (CoA): Comprehensive potency, heavy metal, and microbial testing data for every lot.
  • Certificate of Free Sale (CFS): Officially issued certificates verifying legal commerce within North America.
  • Allergen & GMO Attestations: Clean label documentation including Non-GMO, BSE/TSE, and gluten-free status.
  • Retailer & Marketplace Compliance: Validation testing protocols formatted for Amazon and global distribution channels.
Audited Quality Systems

Globally Recognized Manufacturing Standards

Our facilities undergo strict third-party inspections to verify compliance with FDA regulations and international quality benchmarks.

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
5-Stage Workflow

From Initial RFQ to Final Commercial Dispatch

We maintain a structured onboarding timeline so your product launch stays on budget and on schedule.

  1. Formula Review

    Our technical team reviews raw material availability, excipient compatibility, and target cost objectives.

  2. Price Quotation

    Receive a clear tier-priced quote outlining raw materials, blending, encapsulation, and packaging fees.

  3. Benchtop Sampling

    Our lab crafts pilot bench samples for taste, color, disintegration, and physical specification sign-off.

  4. cGMP Production

    Commercial batching proceeds under ambient-controlled cGMP conditions with in-line testing checks.

  5. QC Release & Ship

    Analytical certificate release followed by export pallet wrapping and freight forwarder coordination.

Procurement Questions

Frequently Asked Questions

Answers to common questions from sourcing professionals and international buyers evaluating Bactolac.

Our technical sales and scientific team reviews RFQ specifications promptly. Standard custom manufacturing quotes are returned within 24 to 48 business hours following preliminary formula review.

To provide an exact cost breakdown, we require your desired dosage form (capsule, tablet, powder, softgel), master formula or active ingredients, serving size, bottle/count configuration, and target order quantity.

Production MOQs generally start at 25,000 units for bottled capsules and tablets, and 1,000 kg for bulk powder blends. Custom pilot volumes for product line launches are evaluated case-by-case.

Yes. We routinely issue full Certificates of Analysis (CoA), Certificates of Free Sale (CFS), allergen statements, Non-GMO declarations, and heavy metal testing reports required by customs authorities worldwide.

Ready to Request Your Manufacturing Quote?

Connect with our technical team today to request a quote, review production capacity, or download our comprehensive manufacturing product catalog.

Get Catalog