Lorazepam Tablets Suppliers & Bulk Manufacturers
Available Forms: Oral Tablets
Available Strengths: 0.5 mg, 1 mg, 2 mg
Reference Brands: Ativan®(US); Tavor®(EU)
Category: Antipsychotropic Drugs
Lorazepam Tablets is available in Oral Tablets and strengths such as 0.5 mg, 1 mg, 2 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, Lorazepam 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) |
Lorazepam 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: Lorazepam tablets (brand name: Ativan) are FDA-approved in the United States for the management of anxiety disorders, short-term relief of anxiety symptoms, and use as a pre-anesthetic. In the European Union, lorazepam is approved under various brand names for similar indications, often governed by national authorizations rather than centralized EMA procedures. As a Schedule IV controlled substance in the U.S., regulatory compliance includes CNS depressant safety labeling, abuse potential warnings, and GMP-certified manufacturing. EU regulations also mandate Risk Management Plans (RMPs) and pharmacovigilance. To explore dossier-ready lorazepam tablets, visit Pharmatradz.com.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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