Fluphenazine Im Injection 25 mg/mL Suppliers & Bulk Manufacturers
Available Forms: Long-Acting Intramuscular Injection
Available Strengths: 25 mg/mL
Reference Brands: Prolixin Decanoate(US); Fluphenazine Decanoate(EU)
Category: Antipsychotropic Drugs
Fluphenazine IM injection is a typical antipsychotic that works by blocking dopamine D2 receptors in the brain, helping to reduce psychotic symptoms like hallucinations, delusions, and agitation. It is primarily used to treat schizophrenia and other chronic psychoses, especially in patients with poor medication adherence.
Product Description: Fluphenazine IM injection, available in both short-acting and long-acting (decanoate) formulations, is FDA-approved in the United States for the treatment of chronic schizophrenia. In the EU, it is approved in select markets under national procedures. Regulatory submissions must meet GMP standards, ensure accurate dosing for depot formulations, and include safety data addressing extrapyramidal symptoms and neuroleptic malignant syndrome. EU applications must align with local pharmacovigilance requirements and psychiatric labeling standards. For global buyers seeking dossier-ready Fluphenazine IM injections and to explore other dosage forms and suppliers, visit Pharmatradz.com — your reliable B2B pharma sourcing platform.
Fluphenazine Im Injection — third party manufacturing & bulk supply
Fluphenazine Im Injection 25 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
Fluphenazine Im Injection is supplied as Long-Acting Intramuscular Injection — an injectable dosage form, so the indicative MOQ is 50,000 units. 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 Fluphenazine Im Injection listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.
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