Zuclopenthixol Ong-Acting Im Injection (Depot) 200 mg/mL, 500 mg/mL Suppliers & Bulk Manufacturers
Available Forms: Long-acting IM Injection (Depot)
Available Strengths: 200 mg/mL, 500 mg/mL
Reference Brands: Clopixol Depot®(US)
Category: Antipsychotropic Drugs
Zuclopenthixol is a typical antipsychotic that works by blocking dopamine (D2) receptors in the brain, reducing psychotic symptoms. It’s primarily used as a long-acting intramuscular injection to manage schizophrenia, particularly in patients with poor medication compliance. It helps maintain symptom control over extended periods.
Product Description: Zuclopenthixol long-acting IM injection, a typical antipsychotic depot formulation, is not FDA-approved in the United States but is widely authorized in the EU under the brand Clopixol Depot. In Europe, it follows EMA guidelines for long-acting injectable neuroleptics, indicated for schizophrenia and related psychoses. EU compliance requires GMP manufacturing, stability data, and pharmacovigilance alignment. U.S. market entry may involve a 505(b)(2) pathway and complete ANDA dossier. To explore dossier-ready forms, formulations, and global suppliers of Zuclopenthixol long-acting IM injection, visit Pharmatradz.com.
Zuclopenthixol Ong-Acting Im Injection (Depot) — third party manufacturing & bulk supply
Zuclopenthixol Ong-Acting Im Injection (Depot) 200 mg/mL, 500 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
Zuclopenthixol Ong-Acting Im Injection (Depot) is supplied as Long-acting IM Injection (Depot) — 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 Zuclopenthixol Ong-Acting Im Injection (Depot) listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.
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