Bactolac Pharmaceutical
Full-service maker of capsules, tablets and powders, including sublingual tablets and enteric-coated capsules.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Bactolac Pharmaceutical operates 650,000 sq ft of manufacturing space in Hauppauge, New York. Founded in 1995, the company is one of the largest full-service supplement manufacturers on Long Island. They handle every step in-house, from product development through final packaging and label application. Bactolac holds independently confirmed NSF GMP certification, and reports additional certifications from UL, NPA, and QAI (USDA-accredited organic certifier). Their product range covers standard capsules and tablets as well as specialty formats like sublingual tablets, enteric-coated capsules, and stick packs. The company has developed expertise in emerging supplement categories including nootropics, longevity products, and pet supplements. They can support brands seeking NSF for Sport, organic, or Non-GMO Project verification for their finished products. Their in-house testing lab runs quality control without relying on outside laboratories.
Certifications
1 of 5 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Capsules · Tablets · Powders · Softgels · Liquids · Sachets
- CAPABILITIES
- Custom formulas · Private label or white label · Packaging · Quality control or lab testing · In-house testing lab · Pet supplements
- DOSAGE FORMS
- capsules · liquids · powders · sachets · softgels · tablets
Sources
- Bactolac Pharmaceutical - Official Website(2026-03-12)
- Bactolac - Certifications(2026-03-12)
- NSF GMP Listing(2026-03-12)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Bactolac Pharmaceutical and other vendors, capabilities, and certifications is in the manufacturer atlas.
Enforcement screening: included in Inventory Ready's most recent completed pass against FDA's published recall datasets (2026-07-09). Method and limits →
Our Evaluation Method
A full assessment applies six checks. Source-Checked listings get a lighter review.
- Independent confirmation: Claims backed by documentation, not marketing copy
- How recent the data is: Information reviewed and dated within the last 12 months
- Sources we traced: Sources cited for every key claim
- Inconsistencies flagged: Where a company's claims and public records disagree, we say so
- What we disclose: Material connections stated directly on affected listings
- What we don't know: When we can't assess something, we say so explicitly
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