Ina Pharmaceutics develops and markets prescription medicines through multi-platform drug-delivery systems, with a portfolio that includes topical corticosteroids and oral therapies. Based in Fairmont, West Virginia, the specialty pharmaceutical company says its product-development and production work follows U.S. Food and Drug Administration current good manufacturing practice regulations.
Current Good Manufacturing Practice (cGMP) regulations enforced by the United States Food and Drug Administration (FDA)
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Modavar Pharmaceuticals, LLCEstablished in 2005, Modavar Pharmaceuticals is a Washington, D.C.-headquartered subsidiary of India’s Cadila Pharmaceuticals and a specialty pharmaceutical company. Its FDA-approved Frederick, Maryland facility gives the company a U.S. base for developing and manufacturing topical products, while its broader work supports pharmaceutical partners serving the U.S. and European markets.GAITHERSBURG, MD
WES Pharma IncFrom its 32,000-square-foot facility in Westminster, WES Pharma Inc develops and manufactures technology-driven specialty generic drugs for U.S. markets, spanning both prescription and over-the-counter products. The privately owned company takes products from in-house research and formulation through FDA approval and manufacturing, with particular focus on technically difficult, niche medicines. Its scientific team works across solid and liquid dosage forms, including products facing solubility, stability, and complex bioequivalence challenges.WESTMINSTER, MD
Greene Street Pharmaceuticals, LLCBased in Pennsylvania, privately held Greene Street Pharmaceuticals develops and manufactures transdermal medicines, taking products from formulation through clinical studies and commercialization in-house. Its distinctive model combines a portfolio of Transdermal Innovative Products with small-scale direct manufacturing capacity of more than 3 million patches annually, focused on the 505(b)(2) pathway and on delivery options for patients with swallowing difficulties. The company operates an FDA-registered facility capable of production under cGMP standards.DOYLESTOWN, PA
Jerome Stevens Pharmaceuticals, IncFamily owned and operated since 1979, Jerome Stevens Pharmaceuticals manufactures prescription tablet and capsule formulations in the United States. The company moved from vitamins and over-the-counter preparations into prescription medicines in 1987, and in 2000 became the first company to receive FDA approval for a branded levothyroxine product, Unithroid®. Today, it continues to emphasize product quality over volume while producing billions of tablets.BOHEMIA, NY