Tramadol Hydrochloride Tablets Suppliers & Bulk Manufacturers
Available Forms: Tablets(IR/ER)/ Capsules
Available Strengths: Capsules, Tablet(IR: 50 mg; ER:00 mg, 200 mg, and 300 mg)
Reference Brands: Ultram(US)
Category:
Active Pharmaceutical Ingredient
Tramadol Hydrochloride is an opioid analgesic that works by binding to mu-opioid receptors and inhibiting reuptake of norepinephrine and serotonin, modulating pain perception. Benefits include effective relief from moderate to severe pain, improved quality of life, and reduced suffering, supporting postoperative recovery and chronic pain management.
Tramadol Hydrochloride tablets is available in Tablets(IR/ER)/ Capsules
and strengths such as Capsules, Tablet(IR: 50 mg; ER:00 mg, 200 mg, and 300 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, Tramadol Hydrochloride 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) |
Tramadol Hydrochloride 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:
Tramadol Hydrochloride is approved in the US and EU, supported by robust dossiers demonstrating safety, efficacy, and manufacturing quality in compliance with GMP and IVDR standards. In the US, FDA regulates tramadol as a Schedule IV controlled substance, requiring strict post-market surveillance. In the EU, CE marking certifies conformity with in vitro diagnostic regulations. These assessments include clinical trial data, safety profiles, and manufacturing audits. For detailed licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to safe, effective tramadol products for pain management worldwide.
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