Abstract: The present invention relates to parenteral emulsion formulations of cannabidiol comprising synthetic cannabidiol (CBD), omega 3 components and other pharmaceutically acceptable excipients. The invention further relates to parenteral emulsion formulations comprising synthetic cannabidiol in combination with one or more active agents, omega 3 components, and other pharmaceutically acceptable excipients. The formulations are used to treat acute and chronic pain, inflammatory conditions, hepatic, cardiovascular disorders, respiratory conditions, immune disorders, and CNS disorders.

Abstract: The present invention relates to a stable, parenteral formulations of naproxen sodium. The formulation further relates to liquid formulations comprising naproxen sodium, cyclodextrin and optionally other pharmaceutically acceptable excipients selected from pH modifying agents, chelating agents and tonicity agents. Also relates to the process of preparing the same. These formulations are stable when stored at recommended storage conditions and can be manufactured using simple manufacturing procedure. These compositions can be used to treat pain, particularly when quicker onset of action is desired. Further the present invention also relates to the parenteral formulations of naproxen in combination with additional active ingredients.

Abstract: Inflammatory disorders of the lung are induced by COVID-19 disease, asthma, and numerous other disorders. Omega-3 fatty acids (O3FA), particularly docosahexaenoic acid (DHA), docosapentaenoic acid (DPA) or cicosapentaenoic acid (EPA), have known anti-inflammatory and pro-resolving properties. Reduction of lung pathology and inflammation will be accomplished by a mixture incorporating O3FA that is suitable for nebulization using formulas and nebulization apparatus known in the art. The O3FA may be delivered in the form of ethyl esters (EE) or free fatty acid (FEA) oils or non-phosphate-containing glycerolipids or as phospholipids (PL) or as any other form known in the art. The mixture can also be delivered in any of the other forms of inhaled droplet or solids for inhalation known in the art. The patient will inhale for a therapeutically effective period of time to reduce inflammation and improve breathing.

Abstract: The present invention relates to a formulation comprising a nano lipid carrier system comprising an active ingredient, low phase transition solid lipid, PEGylated lipid, surfactants and cosolvents etc, dispersed in water or aqueous medium. The hydrodynamic diameter of the nanocarrier system in aqueous media is less than about 1000 nm. The present invention formulation can be in the form of a liquid (solution, suspension, dispersion), liquid filled hard gelatin capsule, soft gelatin capsule or a liquid concentrate.