Ingrédients pharmaceutiques

METOLOSE® SR 90SH-15000SR provides a genuine consistency in Sustained release (matrix tablets). It can be used for semi solid drug products. For Hydrophilic matrix formulation of API and METOLOSE® SR to extend the dissolution. The dosage forms can be obtained by direct compression or granulation process. METOLOSE® SR has specifications of particle size which can be suitable for sustained release application. Dissolution profile can be easily adjusted by selecting appropriate grade. Recommendable amount of METOLOSE® SR is more than 20% in the formulation in order to form the stable gel layer.

MANNITAB SD1 is a spray-dried mannitol with a particle size of 100 microns, commonly used as a diluent in tablet formulations.

ABISORB-DC™ is a co-processed excipient system. It allows manufacturers to make direct compression tablets with liquid lipids and other lipophilic excipients without the need for specialized equipment or processes.

USP-Grade Propylene Glycol is a synthetic, odorless, and colorless liquid widely used in pharmaceutical formulations. It acts primarily as a solvent, humectant, and preservative, making it essential in various dosage forms like oral liquids, injectables, topical creams, and gels. Its ability to dissolve active ingredients, retain moisture, and stabilize formulations helps enhance the efficacy, stability, and shelf life of medications. Additionally, its non-toxic and generally recognized as safe (GRAS) status allows it to be used in oral and topical pharmaceutical products without adverse effects.