Oxycodone tablets bulk supplier for pharma manufacturers

Oxycodone Tablets Suppliers & Bulk Manufacturers

Available Forms: Oral Tablets

Available Strengths: 5 mg, 10 mg, 15 mg, 20 mg, 30 mg, 40 mg, 80 mg

Reference Brands: OxyContin, Roxicodone, Oxymorphone(US); OxyContin, OxyNorm(EU)

Category: Analgesic

Oxycodone binds to mu-opioid receptors in the brain and spinal cord, blocking pain signals and altering perception of pain. It provides effective relief from moderate to severe pain, with benefits including rapid onset, potent analgesia, and improved comfort. When used properly, it offers reliable, long-lasting pain control. Oxycodone tablets is available in Oral Tablets and strengths such as 5 mg, 10 mg, 15 mg, 20 mg, 30 mg, 40 mg, 80 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, Oxycodone 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)

Oxycodone 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.

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📘 Sourcing Guide

Product Description:

Oxycodone tablets are approved in the US and EU for managing moderate to severe pain. In the US, brands like OxyContin and Roxicodone are regulated by the FDA, supported by extensive clinical data, with strict controls due to abuse potential. In the EU, approval by the EMA requires comprehensive dossiers demonstrating safety, efficacy, and manufacturing standards; regulatory oversight includes rigorous risk management plans. Both regions enforce strict regulations, including licensing, prescribing guidelines, and pharmacovigilance. For regulatory dossier preparation, compliance, and registration support, visit PharmaTradz. We assist in seamless market access for oxycodone tablets, ensuring adherence to European and American standards for safe, effective pain management.

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Frequently Asked Questions

Oxycodone is used for the relief of moderate to severe pain. It works as a strong opioid analgesic by acting on the central nervous system to reduce the perception of pain.

Oxycodone is made from oxycodone hydrochloride, a semi-synthetic opioid derived from thebaine, an opiate alkaloid found in the poppy plant.

Common trade names include OxyContin, Roxicodone, and Oxynorm.

OxyContin is marketed by Purdue Pharma, Roxicodone by Mallinckrodt, and Oxynorm by Napp Pharmaceuticals / Mundipharma. Many generic manufacturers also produce oxycodone worldwide.

The generic name is oxycodone hydrochloride.

Well-known brand names include OxyContin, Roxicodone, and Oxynorm.

Oxycodone is manufactured in several countries including India, the USA, and multiple EU regions by both branded and generic pharmaceutical manufacturers.

Yes, Oxycodone tablets is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Oxycodone tablets is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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