Product Testing Lab
Our on-site analytical and microbiological laboratories perform incoming raw material identity verification, heavy metals assay, micro testing, stability testing, and finished product verification on every batch.
When bringing a new dietary supplement to market or scaling up existing product lines, global brand owners, importers, and distributors require a reliable US-based manufacturing partner. Bactolac Pharmaceutical delivers complete turn-key solutions backed by over 30 years of industry leadership in Hauppauge, New York.
Our expansive production capabilities allow us to manage every critical phase of supplement production under one roof. From raw material identity testing and custom formulation development to advanced coating, tableting, encapsulation, and export packaging, we maintain absolute control over product specifications, quality assurance, and delivery schedules.
We streamline supplement manufacturing into a seamlessly integrated single-source workflow, eliminating handoff delays and vendor markups.
Our on-site analytical and microbiological laboratories perform incoming raw material identity verification, heavy metals assay, micro testing, stability testing, and finished product verification on every batch.
Our experienced formulation scientists assist in refining your product concepts. We integrate the latest clinically studied ingredients, optimize bio-availability, and ensure shelf-life stability.
Full-scale packaging capabilities including HDPE/PET bottles, wide-mouth jars, blister packing, gusset bags, stick packs, single-serve pouches, and automated label application with full tamper evidence.
Unmatched expertise in masking unpleasant dietary active flavors, boosting mouthfeel, and engineering clean natural sweetener systems across powders and chewables for international markets.
Whether you need custom contract manufacturing or ready-to-market private label supplement formulations, our multi-line production capabilities cater to every dosage form.
High-shear and ribbon blending for sports nutrition, health, and dietary beverage mixes. Engineered for rapid dissolution, uniform active dispersion, and superior sensory profiles.
High-speed rotary tablet presses capable of producing varied shapes, custom embossing, time-release matrices, and functional coatings engineered for optimal disintegration and absorption.
High-speed encapsulation handling powder, beadlet, and liquid fills. Available in size 000 through size 4 in gelatin, vegetarian, non-GMO, and organic shell options.
Specialized softgel production for lipid-based actives, paired with automated packaging systems designed to protect product integrity during international freight.
Overseas importers and high-growth brands need a manufacturing partner that can absorb market demand spikes without compromising lead times or quality controls.
| Manufacturing Process / Operation | Daily Production Output Capacity |
|---|---|
| Tablet Compression | 35 Million Units / Day |
| Tablet Coating (Film, Enteric, Color) | 25 Million Units / Day |
| High-Shear Powder Blending | 30,000 kg / Day |
| Capsule Encapsulation | 25 Million Units / Day |
| High-Speed Bottling & Labeling | 200,000 Bottles / Day |
| Powder Container Filling | 70,000 Tubs / Day |
| Stick Pack Sachet Packaging | 150,000 Packs / Day |
| Single Serve Pouch Packaging | 120,000 Pouches / Day |
| Blister Packing (Alu-Alu / PVC) | 500,000 Cards / Day |
Choosing the right manufacturing model depends on your brand's speed-to-market priorities, R&D investment budget, and custom intellectual property goals.
Under a custom contract manufacturing agreement, your brand provides the specific formula, raw material grade parameters, and target active levels. Bactolac manufactures strictly to your proprietary Master Manufacturing Record (MMR).
Private label manufacturing allows you to capitalize on Bactolac’s library of pre-formulated, stability-tested, market-proven dietary supplements. You select the packaging, add your custom label, and go to market fast.
Navigating global regulatory standards requires an experienced US manufacturer. Bactolac operates under FDA 21 CFR Part 111 cGMP guidelines and is independently registered by NSF. Every manufacturing run is accompanied by strict quality control documentation required for international shipping and marketplace approvals (including Amazon, retail chains, and international health ministries).
Consumer retention in dietary supplements depends directly on taste and sensory experience. Botanical extracts, vitamins, and minerals frequently possess bitter, astringent, or metallic taste profiles that require sophisticated masking.
Our in-house flavor scientists utilize proprietary masking agents, micronization, and natural flavoring systems (organic fruit powders, stevia, monk fruit, natural aromas) to turn challenging active formulations into pleasant-tasting powders, chewable tablets, and liquids.
Key information for international buyers, importers, and brand owners sourcing supplement contract manufacturing from the USA.
Contract manufacturing involves producing a custom formula designed specifically according to your unique ingredient requirements, active potencies, and brand specifications. Private label manufacturing involves choosing from our library of ready-made, pre-tested, high-quality stock formulas that can be immediately labeled and packaged with your artwork for faster market launch.
Our facility can produce up to 35 million tablets, 25 million capsules, and 30,000 kg of powder daily. Bottling capacity reaches 200,000 bottles per day. Standard lead times typically range between 6 to 10 weeks depending on raw material sourcing and packaging component approvals.
Bactolac operates in full compliance with FDA 21 CFR Part 111 cGMP regulations and holds NSF Registered GMP certification. We are also certified for USDA Organic manufacturing (via QAI) and offer Kosher and Halal production capabilities upon customer request.
Yes. We regularly export to buyers in Europe, Canada, Asia, the Middle East, Australia, and South America. We supply full export documentation including Certificates of Analysis (COA), Certificates of Free Sale (CFS), Allergen Declarations, BSE/TSE statements, and manufacturing process flow charts required by foreign regulatory bodies.
Yes. All of our raw materials and finished goods undergo rigorous analytical assays, heavy metal testing, and microbiological analysis that fulfill Amazon's strict quality assurance documentation guidelines.
Contact our project management team today to review your formulation brief, request a competitive quote, or arrange a facility audit.