Levetiracetam Oral Solution 100 mg/mL Suppliers & Bulk Manufacturers
Available Forms: Oral solution
Available Strengths: 100 mg/mL
Reference Brands: US: Keppra®, Keppra XR®; EU: Keppra®, Levetiracetam Teva®, EpiKeppra®, Zentiva®
Category: Antipsychotropic Drugs
Levetiracetam acts by binding to the SV2A protein in the brain, regulating neurotransmitter release and stabilizing neuronal activity. It is used to treat partial-onset, myoclonic, and generalized tonic-clonic seizures. The oral solution is ideal for pediatric and elderly patients or those with swallowing difficulties.
Product Description: Levetiracetam Oral Solution is FDA-approved in the USA for the treatment of partial-onset, myoclonic, and generalized tonic-clonic seizures in adults and children aged 1 month and older. It complies with GMP standards, includes pediatric-specific dosing, and carries CNS adverse effect warnings. In the European Union, it is approved through national or mutual recognition procedures, requiring detailed Risk Management Plans (RMPs) and Periodic Safety Update Reports (PSURs). Formulations must meet bioavailability and stability criteria. The oral solution is valuable for patients with swallowing difficulties. Explore more formulations of Levetiracetam at Pharmatradz.com.
Levetiracetam Oral Solution — third party manufacturing & bulk supply
Levetiracetam Oral Solution 100 mg/mL is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:
Indicative minimum order quantity
Levetiracetam Oral Solution is supplied as Oral solution — a dosage form priced by order value, so the indicative MOQ is a minimum order value of USD 5,000 per product. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.
Manufacturers of Levetiracetam Oral Solution listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.
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