For over 20 years, Bactolac Pharmaceutical provides turnkey manufacturing services of high-quality Dietary supplements at competitive prices. Founded in New York in 1995, Bactolac helped customers become successful in the health and wellness supplementation market by leading the industry in full-service health supplement manufacturing.
Everything is done in house – from product manufacturing to product testing, packaging and labeling – and is backed by the Bactolac guarantee of the highest in quality standards of compliance.
Meet the people behind the label. Learn more about the staff, scientists, technicians and Dr. Reddy himself.
Our 350,000-square-foot facility is cGMP certified and features advanced equipment for high-volume production.
Finished products are tested on-site in our labs, creating the safest and most effective dietary supplements available today.
Consistency, quality and complete customer satisfaction is the Bactolac advantage.
Bactolac Pharmaceutical is a leader in the nutraceutical industry, specializing in full turn-key nutritional supplement & vitamin contract manufacturing. As a top dietary supplement manufacturing company, we are one of only a few full-service health supplement facilities, offering everything from product manufacturing to product testing, packaging and label application. This is why Bactolac is the best supplement manufacturer for you. We offer each of our customers
cGMP refers to the Current Good Manufacturing Practice regulations enforced by the US Food and Drug Administration (FDA). 21 CFR 111: cGMP in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements are the regulations requiring systems that assure proper design, monitoring, and control of manufacturing processes, packaging processes and facilities.
Adherence to the cGMP regulations assures dietary supplements meet established specifications for identity, purity, strength, composition, and do not exceed their limits for contaminants.
cGMP refers to the Current Good Manufacturing Practice regulations enforced by the US Food and Drug Administration (FDA). 21 CFR 111: cGMP in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements are the regulations requiring systems that assure proper design, monitoring, and control of manufacturing processes, packaging processes and facilities.
Adherence to the cGMP regulations assures dietary supplements meet established specifications for identity, purity, strength, composition, and do not exceed their limits for contaminants.
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