प्रीगैबलिन एपीआई

Pregabalin EP Powder refers to Pregabalin that meets the European Pharmacopoeia EP standards in its powdered raw form Its typically used in the pharmaceutical industry for manufacturing medications particularly capsules and tablets What is Pregabalin Drug Class Anticonvulsant Neuropathic pain agent Mechanism of Action Binds to the alpha2delta subunit of voltagegated calcium channels in the central nervous system reducing neurotransmitter release and excitability EP Powder What it Means EP European Pharmacopoeia A quality standard that ensures the identity purity strength and consistency of pharmaceutical substances in Europe Powder form Indicates its a raw active pharmaceutical ingredient API not yet formulated into a dosage form like a capsule or tablet Common Uses When Formulated Neuropathic pain eg diabetic neuropathy postherpetic neuralgia Fibromyalgia Partial seizures as adjunctive therapy Generalized anxiety disorder GAD approved in some countries Key Chemical Properties Molecular Formula CHNO Molecular Weight 15923 gmol Appearance White to offwhite crystalline powder Solubility Freely soluble in water Storage and Handling Store in a tightly closed container at controlled room temperature Protect from light and moisture Handle in a controlled pharmaceutical environment using appropriate PPE Regulatory Notes Manufacturers must comply with Good Manufacturing Practices GMP The EP monograph for Pregabalin outlines specific testing criteria for Identification Impurity profile Assay content Residual solvents Microbial limits