Powder Manufacturing
High-shear and ribbon blending for protein, collagen, hydration, greens and pre-workout formulas. Flavor masking, particle-size control and bulk or unit-dose filling.
Since 1995 · New York, USA
Vitamin & Health Supplement Manufacturer
Turn-key contract manufacturing for powders, capsules and tablets — formulated, tested, packaged and labeled under one cGMP roof.
30+Years Manufacturing
200,000+Sq. Ft. Production Space
2On-Site QC Laboratories
1Single-Source Supply Chain
Welcome to Bactolac
A Full-Service Dietary Supplement Manufacturer Global Brands Rely On
Founded in New York in 1995, Bactolac Pharmaceutical has spent more than three decades helping health and wellness brands move from concept to shelf-ready product. Our teams have executed tens of thousands of production runs across vitamins, minerals, botanicals, probiotics, amino acids and functional powders.
Because formulation, blending, encapsulation, tableting, analytical testing, packaging and label application all happen inside our own facilities, your project is never handed off to an unknown subcontractor. That single-source control is what keeps specifications tight, documentation complete and launch dates predictable.
- Dedicated project manager from formulation brief to final pallet
- In-house R&D for custom, clean-label and clinically inspired formulas
- Documentation packages built for retail, Amazon and export compliance
Core Capabilities
Manufacturing Services Built Around Your Dosage Form
Choose a single delivery format or build a complete product family. Equipment, tooling and validated processes are already in place — so scale-up does not mean starting over.
Capsule Manufacturing
Vegetarian and gelatin two-piece capsules, size 000 to 4, plus liquid-filled, banded and delayed-release options for sensitive actives and probiotic strains.
Tablet Manufacturing
High-speed compression with bi-layer, chewable, sublingual, effervescent, enteric and time-release technologies, plus color coating and pharmaceutical glaze.
Contract & Private Label
Launch faster with proven base formulas, or protect a proprietary blend under strict confidentiality. Both routes include label review and artwork application.
Nutritional Supplements
Multivitamins, minerals, omegas, joint, immune, sleep and digestive support — developed with realistic overages and verified stability data.
Tour Our Facilities
Audit-ready plants with controlled airflow, segregated allergen handling and sampling booths. In-person and virtual buyer audits are welcomed.
High-Growth Categories
Where Our Formulation Experience Creates Advantage
Category knowledge shortens development cycles. These are the segments our scientists work in every week — including the ingredient sourcing, sensory and stability challenges unique to each.
Vitamins & Minerals
Chelated minerals, methylated B-vitamins and bioavailability-focused blends with documented potency at end of shelf life.
Sports Nutrition
Pre-workout, intra-workout and recovery systems: creatine, EAAs, beta-alanine, electrolytes and protein matrices.
Herbal & Botanical
Standardized extracts and whole-herb powders with identity verification, solvent screening and organic-certified options.
Longevity & Anti-Aging
NAD⁺ precursors, resveratrol, spermidine and cellular-health stacks formulated for stability and clean labeling.
Women’s Health
Hormone balance, menopause comfort, prenatal and beauty-from-within formats with gentle-on-stomach mineral forms.
Pet & Animal Health
Palatable powders, soft chews and tablets for joint, calming, skin and coat programs in companion-animal channels.
Functional Beverages
Cold-water dispersible hydration and superfood mixes engineered for clarity, mouthfeel and stick-pack accuracy.
Everyday Wellness
Immune, sleep, gut and cognitive support built on transparent dosing that survives retailer and marketplace scrutiny.
Inside Our Plant
See How a Formula Becomes a Finished Bottle
Walk the floor with us: raw material quarantine, weighing and dispensing, blending, encapsulation and tableting, in-process checks, bottling and label application.
Quality & Compliance
Evidence, Not Claims: How We Prove Every Batch
Under FDA 21 CFR Part 111, a dietary supplement manufacturer must establish specifications for identity, purity, strength and composition — and then prove each one. Our quality system is designed so that proof is available before a batch is released, not after a complaint.
- Raw material control: quarantine, vendor qualification and identity testing on incoming lots
- In-process verification: blend uniformity, weight variation, hardness and disintegration checks
- Finished product release: potency assay, heavy metals and microbial limits from our own labs
- Traceability: master manufacturing records, batch records and retain samples for shelf-life study
- Marketplace readiness: test panels aligned with major retailer and Amazon documentation requests
Authority & Trust
Independently Audited Certifications
cGMP refers to the Current Good Manufacturing Practice regulations enforced by the U.S. Food and Drug Administration. Adherence assures that dietary supplements meet established specifications for identity, purity, strength and composition — and do not exceed contaminant limits. Bactolac layers voluntary third-party programs on top of that baseline.
Working With Us
A Five-Stage Path From Brief to Bulk Shipment
Overseas buyers and domestic brands follow the same transparent workflow, with defined deliverables and sign-offs at each gate.
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Discovery
Share your target market, dosage form, claim strategy, budget and timeline. We flag regulatory and sourcing risks early.
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Formulation
R&D builds the formula, confirms excipient compatibility and issues a specification sheet with cost per unit.
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Sampling
Pilot or bench samples for organoleptic review, plus accelerated stability screening when required.
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Production
Scheduled batch under cGMP controls, with in-process checks and full batch-record documentation.
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Release & Ship
QC release, Certificate of Analysis, packaging, labeling and export paperwork prepared for your freight forwarder.
Clean Label & Superfoods
Superfood, Organic and Clean-Label Production
Bactolac is licensed and equipped to manufacture superfood products — greens and red-berry blends, mushroom powders, fiber matrices and plant protein systems — with organic-certified lines available.
- Allergen-segregated scheduling and validated cleaning between runs
- Non-GMO, vegan, gluten-free and organic ingredient sourcing support
- Natural flavor and sweetener systems that keep panels short and readable
- Stick packs, single-serve sachets, jars, bottles, blisters and gusset bags
Why Bactolac
More Than a Contract Manufacturer — A Product Development Partner
We serve large, mid-size and emerging brands with the same technical depth: qualified chemists and technicians who can refine a customer’s specific formulation, plus micro and analytical laboratories that let us test comprehensively in-house.
Three Decades of Batch Records
Since 1995 we have solved blend segregation, capsule fill weight drift, tablet friability and flavor fade problems — so your project benefits from precedent, not guesswork.
Scientists On Your Side of the Table
Formulators, analytical chemists and microbiologists collaborate directly with your team on actives, overages, excipients and shelf-life strategy.
Audit-Ready Documentation
Master and batch manufacturing records, specification sheets, allergen and GMO statements, and Certificates of Free Sale for cross-border trade.
One Roof, One Accountability
Blending, dosing, testing, bottling and labeling stay in-house. Fewer handoffs means fewer deviations and a clearer chain of custody.
Capacity That Grows With You
High-capacity production lines absorb seasonal spikes and marketplace promotions without forcing you to re-qualify a new supplier.
Global Buyer Support
Export-savvy project managers coordinate specification translation, artwork compliance checks and freight-ready documentation.
Buyer Questions
Frequently Asked Questions
Practical answers for sourcing managers, brand owners and product developers evaluating a U.S. supplement manufacturer.
Yes. Our in-house R&D chemists and formulation scientists develop, benchmark and stability-screen custom formulas. We evaluate raw material identity, overage requirements, excipient compatibility, flowability and organoleptics before a pilot batch is scaled to full production — so the product that ships behaves like the sample you approved.
Production MOQs typically start around 25,000 units for tablets and capsules and 1,000 kg for powder blends, with pilot and launch volumes reviewed case by case. Standard lead times run six to ten weeks after approval of the formula, specification sheet and packaging components. Raw material availability — particularly for branded or standardized botanical extracts — is the most common variable, so we confirm sourcing during quoting.
Our New York facilities operate under FDA 21 CFR Part 111 cGMP and are NSF registered for Good Manufacturing Practices. We also maintain organic certification through Quality Assurance International, hold Natural Products Association membership, and can produce Kosher and Halal certified supplements on request. Full certificate copies are available for buyer audit files.
Our regulatory-experienced team reviews supplement facts panels, serving sizes, ingredient nomenclature, allergen declarations and structure/function claim language before artwork is finalized. Working alongside your team helps avoid relabeling delays, customs holds and marketplace listing rejections.
Standard export packages include Certificates of Analysis, Certificates of Free Sale, manufacturing flow charts, specification sheets, allergen and GMO statements, BSE/TSE declarations, and heavy-metal and microbiological test results. Additional country-specific attestations can be prepared on request.
Yes. Bottles, wide-mouth jars, gusset bags, boxes, blisters, stick packs and single-serve pouches are filled, sealed and labeled in-house, including tamper-evident and child-resistant closures. Cases can be configured with the carton counts, inner packs and labeling formats your retailer or marketplace requires.
Ready to Build Your Next Product?
Send us your dosage form, target market and volume expectations. A project manager will respond with a technical feasibility review and a clear next step.