Bi-Layer Tablets
Separate incompatible ingredients or combine immediate-release and extended-release layers into a single dual-color tablet format for enhanced bioavailability.
When expanding your brand into international retail channels or online marketplaces, product quality, dosage accuracy, and regulatory compliance are non-negotiable. At Bactolac Pharmaceutical, Inc., we specialize in high-capacity contract tablet manufacturing, producing premium dietary supplements that meet rigorous global standards.
Operating from our 200,000+ sq. ft. cGMP-certified facility in New York, USA, our expert formulation scientists and analytical lab technicians oversee every phase of production. From raw material milling and high-shear granulation to precision compression and specialized coating, we maintain complete control under one roof to deliver consistent, market-ready tablet solutions.
Our automated high-speed tablet presses accommodate diverse shapes, sizes, colors, and functional delivery systems tailored to your brand's specific consumer needs.
Separate incompatible ingredients or combine immediate-release and extended-release layers into a single dual-color tablet format for enhanced bioavailability.
Formulated with custom natural flavors, organoleptic masking, and optimized texture—ideal for multivitamins, kids' nutrition, and stomach-friendly mineral applications.
Fast-dissolving sublingual tablets engineered for direct mucosal absorption, perfect for Vitamin B12, melatonin, and targeted botanical actives.
Specialized pH-sensitive polymer coatings protect sensitive enzymes, probiotics, or botanicals from acid degradation while preventing gastric discomfort.
Hydrophilic matrix technology controls ingredient dissolution over extended hours, ensuring stable, steady nutrient absorption throughout the day.
Precision-engineered effervescent formulas for rapid dissolution in water, delivering instant drinkable electrolytes, vitamin C, and energy blends.
Substandard manufacturing leads to batch rejection, weight variation, and friability issues. Our strict compliance under FDA 21 CFR Part 111 cGMP regulations ensures every tablet lot produced achieves verified potency, purity, and physical stability.
Bactolac Pharmaceutical serves brand owners, distributors, and pharmaceutical importers across North America, Europe, Asia, the Middle East, and Latin America. We understand the complex international trade standards required for seamless entry into your target market.
Our dedicated regulatory support team assists with compliant label artwork formatting, ingredient allowance checks, and standardized export documentation packages needed by foreign customs agencies.
Our facility holds recognized certifications ensuring compliance with U.S. federal guidelines and voluntary quality management standard programs.







A transparent, milestone-driven development process from formula refinement to container shipment.
Collaborative consultation on actives, target dosage, excipient flowability, and market registration targets.
R&D benchtop batching, hardness checks, disintegration testing, and sensory taste sign-off for chewables.
Quarantined ingredient weighing, fluid-bed or wet/dry granulation, and high-shear blend uniformity checks.
High-speed rotary press compression followed by protective aqueous film coating or enteric sealing.
On-site lab assay clearance, bottle or blister filling, packaging, labeling, and export dossier release.
Direct technical answers for commercial sourcing teams, distributors, and brand founders.
We formulate and manufacture bi-layer, chewable, sublingual, effervescent, time-release, enteric-coated, and film-coated tablets. Our team assists with custom shapes, sizes, break-lines, and organoleptic flavor profiles tailored to your brand strategy.
Production MOQs generally start around 25,000 to 50,000 finished bottled units or bulk powder/granulation equivalent. Pilot launch volumes can be evaluated based on raw material availability and specific tooling requirements.
Yes. We routinely prepare comprehensive international export packages including Certificates of Analysis (CoA), Certificates of Free Sale, allergen declarations, non-GMO statements, BSE/TSE declarations, and manufacturing flow diagrams for international customs clearance.
Our technicians perform strict in-process control testing at regular intervals during tablet compression. We measure tablet weight variation, thickness, hardness, friability, and disintegration rates to ensure every batch aligns strictly with master specifications.
We offer automated packaging in HDPE and PET bottles, glass jars, blister packs, unit-dose pouches, and gusset bags with tamper-evident induction seals, cotton fillers, and child-resistant closures.
Discuss your tablet formulation, target market requirements, and batch size with our technical project managers today.