A Leading Developer and Manufacturer of Affordable, High-Quality Generic Pharmaceuticals.

Qualitest meets the needs of today’s healthcare customers by providing affordable, high-quality generic pharmaceuticals that provide new op...
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Featuring a current portfolio exceeding 600 products.

Ranked 5th in the United States for Total Generic Prescriptions Dispensed for the year ending June 2014.
Source: IMS Health

CURRENT MARKET PRODUCTS
Approximately 700 plus total SKUs covering multiple therapeutic classes including: pain, oral contraceptives, cough/cold and muscle relaxants.

PIPELINE
Robust Pipeline across various therapeutic categories.

FACILITIES
Qualitest Pharmaceuticals consists of four state of the art facilities, three in Huntsville, AL and one in Charlotte, NC. The first of the Huntsville facilities is a 180,000 square foot ultra modern facility for the manufacturing and packaging of liquids and other soft products complete with labs for Quality Control (QC) and Research & Development (R&D). The second building is a 280,000 square foot manufacturing and packaging plant for solid dose products, also complete with QC and R&D labs. The third building is 320,000+ square feet, and houses the Qualitest corporate offices, as well as a state of the art distribution facility with the most advanced automated shipping systems.
Our Charlotte facility is an 88,000+ square foot solid dose manufacturing and packaging facility with innovative high velocity equipment. This facility also includes laboratory space for QC and R&D.

PRODUCTS
Our extensive range of prescription and over-the-counter products comprises of tablets, capsules, liquids, suspensions, creams, and ointments. We offer products in a wide variety of therapeutic categories, including antihypertensives, analgesics, antibiotics, cough/cold, antidepressants, antipsychotics, as well as others. Consumers can find our products at major retailers, as well as locally owned and operated pharmacies.

ABOUT GENERICS
Generic drugs contain the same active ingredient as their brand-name equivalent, but are usually much less expensive. When a new drug is developed, it is protected by a patent for a certain time period, giving the developer exclusive rights to manufacture and sell the product, enabling them to recoup the cost of research and development.

When the patent expires, a generic manufacturer may make a product using the same active ingredient. After stability testing and bioavailability studies to successfully establish equivalence to the branded product, and upon receipt of FDA approval, the company can take it to market. The savings generated through bypassing the clinical research are duly passed along to the consumer.

Generic drugs offer consumers several benefits over brand-name equivalents by:
• Costing less;
• Complying with FDA standards by having the same active ingredients, safety and efficacy profile;
• Treating the same conditions or illnesses;
• Having the same dosage, strength, and means of Administration.


For more information on generic drugs, visit the FDA’s Office of Generic Drugs page.