Chlorpromazine Tablets Suppliers & Bulk Manufacturers
Available Forms: Oral Tablets
Available Strengths: 10 mg, 25 mg, 50 mg, 100 mg, 200 mg
Reference Brands: Thorazine®(US); Largactil®(EU)
Category: Antipsychotropic Drugs
Chlorpromazine is a typical antipsychotic that blocks dopamine D2 receptors in the brain, helping to reduce psychotic symptoms such as hallucinations, delusions, and agitation. It also affects histamine, adrenergic, and muscarinic receptors, providing sedative and antiemetic effects. Chlorpromazine tablets are used to treat schizophrenia, bipolar disorder, severe behavioral problems, nausea, and intractable hiccups. Chlorpromazine Tablets is available in Oral Tablets and strengths such as 10 mg, 25 mg, 50 mg, 100 mg, 200 mg. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Chlorpromazine Tablets is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.
| Technical Specifications & Supply Details | |
|---|---|
| Lead Time | 7 to 60 days (depending on batch size & schedule) |
| MOQ | As per manufacturer’s batch size |
| COA | Available with every batch |
| Regulatory Dossier / DMF | Available upon request |
| Export Documentation | FSC, COA, Manufacturing License, Product Permission |
| Standards | IP, BP, USP |
| Certifications | WHO-GMP, EU-GMP, USFDA (as applicable) |
Chlorpromazine Tablets can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.
Product Description: Chlorpromazine tablets are FDA-approved in the United States for the treatment of schizophrenia, bipolar disorder, severe behavioral issues, nausea, and intractable hiccups. In the European Union, they are available in select countries through national authorization procedures. Regulatory compliance requires GMP manufacturing, bioequivalence data, and robust safety documentation addressing sedation, extrapyramidal symptoms, and cardiovascular effects. U.S. submissions must align with FDA psychiatric drug labeling and pharmacovigilance standards. EU applications often require country-specific labeling and risk management plans. To explore dossier-ready Chlorpromazine tablets and alternative forms, visit Pharmatradz.com — your trusted B2B pharmaceutical sourcing platform.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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