KVK-TECH, INC. develops and manufactures high quality pharmaceuticals.

The 33,000 square foot (Capacity to expand up to 65,000 square foot) state of the art facility is located in Pennsylvania. It is organized to accommodate the entire business operation including product development, manufacturing, packing/labeling and quality control laboratory. Manufacturing operations, facilities and documentation comply with current good manufacturing practices (cGMP’s).

KVK-TECH is registered with Food and Drug Administration (FDA), Drug Enforcement Administration (DEA) and Department of Environmental Protection (DEP).

The company is committed to developing solid dosage forms that include immediate and modified release tablets, capsules, liquids and semisolid dosage forms. Our products are available throughout the United States from Pharmaceutical wholesalers, distributors, chain drug stores and managed care organizations.

The business environment in which KVK-TECH participates is dynamic. External factors such as population demographics and healthcare funding/expenditures continue to present new challenges. The organization is dedicated to meeting the present and future needs of the healthcare marketplace. Correspondingly, it has allocated substantial resources to aggressively pursue the development of off-patent pharmaceutical products and new modified release products. The company’s employees are devoted to the application of sound scientific fundamentals and make a worthwhile contribution to the well being of consumers.