Partner directly with an established FDA 21 CFR Part 111 cGMP compliant dietary supplement contract manufacturer located in New York, USA. Whether you are scaling an existing nutraceutical product line, developing custom formulations, or seeking full export support, our technical experts and account coordinators are ready to support your business goals.
7 Oser Avenue, Hauppauge, NY 11788-3808, USA
Direct Phone: (631) 951-4908 | Toll Free: 1-800-585-2546
Monday – Friday: 8:30 AM – 5:30 PM (EST)
We simplify cross-border nutraceutical procurement by providing complete batch documentation, certified manufacturing standards, and end-to-end technical transparency.
Standard export paperwork packages include Certificate of Analysis (CoA), Certificate of Free Sale (CFS), BSE/TSE declarations, allergen statements, non-GMO verifications, and master flow charts tailored to your country's customs regulations.
Our 200,000+ sq. ft. Hauppauge manufacturing complex operates under strict US FDA 21 CFR Part 111 cGMP regulations and maintains voluntary NSF registered Good Manufacturing Practices credentials.
In-house quality control chemists perform identity testing on incoming raw materials, in-process weight and disintegration checks, finished product potency assays, and heavy metal screening for every lot.
Reach out to dedicated department heads to streamline product development, quality compliance, and freight forwarding.
Collaborate with formulation chemists to optimize active ingredient bioavailability, organoleptic profiles, excipient compatibility, and dosage forms across capsules, tablets, and powders.
Access master batch manufacturing records, finished product specifications, stability testing data, and comprehensive paperwork needed for marketplace verification.
Coordinate containerized sea freight, air freight shipments, bulk ingredient packaging, and custom palletization directly with our international logistics coordinators.
Essential answers for sourcing managers, purchasing directors, and brand developers contacting Bactolac.
To expedite technical review and quotation, please provide your targeted dosage format (capsules, tablets, or powder blend), active ingredient specifications or formula brief, projected order volume, primary packaging preferences (bottles, gusset bags, stick packs), and final destination market.
All technical inquiries are evaluated by an account coordinator within 24 to 48 business hours. Our team will review your specifications, ingredient availability, and manufacturing requirements before initiating a introductory consultation.
Yes. We welcome qualified international brand owners and retail buyers to inspect our Hauppauge, New York manufacturing plant. Both in-person facility audits and virtual guided plant tours can be arranged through your dedicated account manager.
Connect with our US manufacturing team to receive technical assistance, request sample batches, or initiate contract manufacturing.