Turnkey Custom Vitamin Formulation, In-House Testing & High-Volume Production for Global Brands
As a leading U.S.-based contract vitamin manufacturer with over 30 years of industry experience, Bactolac Pharmaceutical delivers premier custom formulation, blending, encapsulation, tableting, laboratory testing, and turnkey packaging for health and wellness brands worldwide.
Our expansive 650,000 square foot, climate-controlled facility in New York operates in strict adherence to FDA 21 CFR Part 111 cGMP regulations and holds prestigious NSF Good Manufacturing Practices registration. By keeping all formulation, raw material handling, dosage production, analytical testing, and final bottling under one roof, we eliminate subcontractor delays and maintain complete chain-of-custody integrity.
We work with brand owners, distributors, and pharmaceutical importers to transform complex nutritional concepts into shelf-ready, commercially viable vitamin products.
Two-piece hard-shell capsules in vegetarian (HPMC) and gelatin options (sizes 000 to 4). Advanced capabilities include liquid-filled hard capsules, softgels, liposomal suspensions, and delayed-release profiles for maximum intestinal absorption.
High-speed tablet presses producing chewables, sublinguals, bi-layer tablets, effervescents, enteric-coated formulas, and controlled time-release matrices, complete with organic color coatings and pharmaceutical glaze.
Ribbon and high-shear blending engineered for uniform active distribution. Ideal for multivitamins, electrolyte drink mixes, and functional beverage blends packed into wide-mouth jars, stick packs, or single-serve sachets.
Our experienced formulation scientists and biochemists build high-potency, bioavailability-focused vitamin products tailored to consumer demand across global health channels.
Balanced daily wellness stacks utilizing chelated minerals, methylated B-vitamins (L-5-MTHF), and bioavailable trace elements.
High-dose Vitamin C, Vitamin D3/K2, Zinc picolinate, and botanical extracts formulated for rapid systemic uptake.
Brain-active B-complexes, fat-soluble antioxidants, and neuro-protective cofactor blends designed for mental clarity and focus.
Targeted B-12 sublinguals, CoQ10 matrices, and cellular metabolic enhancers built for sports nutrition and daily vitality.
Gender-specific formulations addressing hormonal balance, prenatal care, bone density, and age-related vitality.
Biotin, Vitamin C, Collagen cofactors, and antioxidants formulated for hair, skin, and nail strength.
Enhanced-bioavailability liquid delivery systems engineered for delicate actives requiring mucosal absorption.
Proprietary vitamin combinations tailored specifically to your brand’s unique positioning and regional compliance needs.
Testing delays can severely hamper product rollout schedules. Bactolac Pharmaceutical operates dedicated on-site quality control and analytical laboratories to verify safety, purity, and potency at every stage of production.
Our team of analytical chemists and microbiologists conducts rigorous testing protocols on incoming raw ingredients, intermediate blends, and finished products, ensuring total alignment with U.S. and international regulatory standards.
Exporting dietary supplements into international markets requires rigorous documentation and full regulatory adherence. Bactolac Pharmaceutical routinely supports overseas importers and global distributors with complete compliance paperwork.
Every batch is accompanied by an extensive, lab-verified CoA confirming active ingredient assay levels, heavy metal limits, and microbial safety.
We supply official U.S. Certificates of Free Sale, BSE/TSE-free attestations, allergen declarations, and non-GMO statements for border regulatory entry.
Individually sealed bottles, wide-mouth jars, blister packs, and fulfillment-ready master carton configurations labeled for global distribution.
Technical guidance for product managers, procurement officers, and brand owners sourcing a contract vitamin manufacturer.
We manufacture custom vitamins across multiple dosage formats including gelatin and vegetarian two-piece capsules (sizes 000 to 4), softgels, liquid-filled hard capsules, tablets (chewable, sublingual, effervescent, bi-layer, enteric-coated, time-release), and functional powder blends packed into bottles, jars, stick packs, or gusset bags.
Our in-house R&D team calculates precise active ingredient overages based on accelerated and real-time stability testing data. Furthermore, every manufacturing run undergoes HPLC potency assays and FTIR identification in our U.S. laboratories to ensure the finished product meets 100% of label claims throughout its shelf life.
Yes. We regularly support global buyers with full export compliance packages including batch Certificates of Analysis (CoA), Certificates of Free Sale, BSE/TSE declarations, allergen statements, GMO attestations, master manufacturing records, and customs-ready packing documentation.
Our typical production MOQs start around 25,000 to 50,000 units for tablets and capsules, and 1,000 kg for custom powder blends. Initial pilot runs and new product launch volumes are evaluated on a case-by-case basis during commercial quoting.
Absolutly. Our team of formulation scientists collaborates directly with your product developers to design custom ingredient profiles, select optimal excipients, optimize organoleptic flavor profiles, and balance cost-efficiency with maximum nutritional efficacy.
Connect with our technical team today to discuss your formula specifications, delivery formats, estimated volumes, and export documentation needs.