NAD+ & Nicotinamide Riboside (NR)
Engineered with active overage calculations and micro-encapsulation techniques to maintain molecular stability and combat degradation over time.
As nutritional science accelerates, cellular longevity and anti-aging supplements have quickly emerged as one of the highest-growth categories in global health markets. Brands worldwide require high-precision manufacturing to ensure sensitive active molecules remain stable, bioavailable, and fully potent from production line to retail shelf.
At Bactolac Pharmaceutical, our 30+ years of contract manufacturing heritage allows us to translate cutting-edge scientific research into shelf-ready, compliant products. Operating out of our state-of-the-art New York facilities under strict U.S. FDA 21 CFR Part 111 cGMP regulations, we offer custom formulation, encapsulation, tableting, and packaging engineered specifically for anti-aging brands targeting North America, Europe, Asia, and Australia.
Our formulation scientists and Ph.D. chemists work directly with global distributors, sourcing managers, and brand owners to build proprietary stacks or high-purity single-ingredient products.
Engineered with active overage calculations and micro-encapsulation techniques to maintain molecular stability and combat degradation over time.
High-purity Trans-Resveratrol paired with synergistic polyphenols and bio-availability enhancers for maximum systemic absorption.
Standardized botanical extracts verified for exact polyamine concentrations, ideal for cellular renewal and autophagy-focused product lines.
Targeted cellular energy stacks formulated to protect mitochondrial membrane integrity and reduce oxidative stress markers.
High-potency botanical senolytics processed through high-shear blending to optimize particle distribution and gut uptake.
Advanced next-generation longevity actives sourced from audited suppliers and validated for heavy metal and contaminant purity.
Different cellular health molecules demand distinct physical delivery mechanisms to optimize targeted release and protect sensitive compounds from stomach acid oxidation.
We provide standard gelatin, HPMC vegetable capsules, chlorophyll vegetarian options, and specialized delayed-release (DRcaps®) designed to survive gastric acid and bypass early enzymatic breakdown.
Our high-speed rotary presses produce bi-layer tablets, chewables, enteric-coated tablets, and fast-dissolving sublingual formats engineered for mucosal absorption.
Clean-label, cold-water-dispersible powders packaged into single-serve stick packs, sachets, or wide-mouth PET/HDPE containers.
In anti-aging supplement sourcing, trust is built on verifiable chemical data. Bactolac maintains two on-site quality control laboratories staffed by qualified chemists and microbiologists to test every production stage.
Raw materials are segregated and identity-confirmed using Spectrographic FT-IR before release into production inventory.
High-Performance Liquid Chromatography (HPLC) verifies active active assay levels meet exacting finished-product claims.
ICP-MS screening ensures heavy metals (Lead, Cadmium, Arsenic, Mercury), residual solvents, and pesticides stay below FDA and EU thresholds.
Pathogen testing for Salmonella, E. coli, Staphylococcus aureus, yeast, and mold before batch clearance.
Importing dietary supplements into international markets requires flawless documentation and adherence to local health authorities. Bactolac routinely supports buyers across Europe, Asia-Pacific, the Middle East, and Latin America.
Technical and procurement answers for brand owners and sourcing managers introducing longevity products.
Every incoming lot of raw materials undergoes quarantine and rigorous analytical identity, purity, and potency testing in our on-site micro and analytical laboratories. We utilize HPLC and FT-IR spectrographic analysis to verify active assay levels before releasing raw materials to production lines.
We offer delayed-release vegetarian capsules (DRcaps®), acid-resistant enteric-coated tablets, bi-layer time-release tablets, sublingual tablets, liquid-filled hard capsules, and clean-label powder drink mixes packaged into stick packs, sachets, or wide-mouth jars.
Yes. We issue complete documentation packages for international buyers, including Certificates of Analysis (CoA), Certificates of Free Sale, BSE/TSE-free statements, allergen declarations, GMO attestations, and manufacturing process flow charts required for cross-border customs and health department registration.
Our R&D formulation team evaluates chemical stability, excipient interactions, and active degradation rates. We calculate precise active overages, utilize specialized low-humidity encapsulation suites, and recommend protective packaging (such as amber glass, desiccant liners, or blister foils) to preserve potency throughout product shelf life.
Partner with a trusted U.S. cGMP contract manufacturer. Contact our technical sales team today to request a product catalog, request a quote, or schedule a facility audit.