Tramadol Hydrochloride structure
Human APIs

Tramadol Hydrochloride

CAS Registry Number: 36282-47-0

Tramadol Hydrochloride is a centrally-acting synthetic opioid analgesic combining weak mu-opioid receptor agonism with serotonin-norepinephrine reuptake inhibition (SNRI activity). Manufactured to USP and Ph. Eur. monograph specifications a

Product information

Tramadol Hydrochloride is a centrally-acting synthetic opioid analgesic combining weak mu-opioid receptor agonism with serotonin-norepinephrine reuptake inhibition (SNRI activity). Manufactured to USP and Ph. Eur. monograph specifications as the racemic mixture of (+)- and (−)- enantiomers, with both isomers contributing to analgesia via distinct mechanisms. Schedule IV in US (federally, since 2014) with lower diversion risk than pure mu-agonists.

Product specifications

CAS Registry Number
36282-47-0
Therapeutic Category
Human APIs
API Technology
Synthetic / Semi-synthetic (per molecule)
Development Status
Commercial — stocked
Manufacturer
Longshine Boi-Tech Pvt. Ltd.
Facility
Pune, Maharashtra, India 411001

Regulatory filings & documentation

We maintain regulatory dossiers in the following jurisdictions for Tramadol Hydrochloride-relevant molecules. Letter of Authorization (LoA) and CEP / DMF / ASMF references are issued at no charge to qualified buyers.

US FDA DMF (Type II)
EDQM CEP (where applicable)
Brazil ANVISA
Canada Health Canada
Japan PMDA
Korea MFDS
GCC SFDA
EU CEP
WHO-GMP & ISO 9001:2015 certified. US FDA Drug Master File available. EDQM CEP supplied for EU procurement. Pharmacopoeial release against USP, Ph. Eur., IP, JP. CoA on every batch. First-shipment lead time 7-10 business days for stocked APIs.
View interactive page & request quote Email sales Order a sample

Frequently asked questions about Tramadol Hydrochloride

What is Tramadol Hydrochloride used for?

Tramadol Hydrochloride is supplied as a pharmaceutical-grade human apis for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using Tramadol Hydrochloride typically reference it under CAS Registry Number 36282-47-0.

What quality and regulatory standards does Longshine Boi-Tech's Tramadol Hydrochloride meet?

Our Tramadol Hydrochloride is manufactured under WHO-GMP and ISO 9001:2015 conditions in Pune, India. Per-batch Certificate of Analysis (CoA) is released against USP / Ph. Eur. / IP / JP specifications depending on destination market. We hold US FDA Drug Master File and EDQM Certificate of Suitability dossiers for the molecules where regulatory recognition is required; Letter of Authorization (LoA) is issued at no charge to qualified buyers.

How do I request a quote, sample, or proforma invoice for Tramadol Hydrochloride?

Quote requests for Tramadol Hydrochloride are turned around within 24 business hours (IST, Pune). Bulk APIs typically ship within 7-10 business days of confirmed PO; air freight to North America and Europe runs 4-5 days door-to-door. Sample agreements are signed before shipping QC-grade material to your formulation laboratory.

Which countries does Longshine Boi-Tech supply Tramadol Hydrochloride to?

We export Tramadol Hydrochloride to 50+ countries including the United States, Canada, Mexico, Brazil, the European Union, the United Kingdom, Japan, Australia, South Korea, the GCC and across South-East Asia. All regulatory documents (DMF / CEP / LoA) and shipping incoterms (EXW, FCA, CIP, DAP, DDP) are negotiated per buyer.

Related Human APIs APIs

Other human apis molecules from Longshine Boi-Tech's WHO-GMP catalogue — each with active regulatory filings, audit-ready CoA, and samples available under CDA.

Naproxen Sodium
CAS 26159-34-2
Levothyroxine Sodium
CAS 25416-65-3
Amoxicillin Trihydrate
CAS 61336-70-7
Paclitaxel
CAS 33069-62-4
Timolol Maleate
CAS 26921-17-5
Fluticasone Propionate
CAS 80474-14-2
Doxorubicin HCl
CAS 25316-40-9
Nalbuphine Hydrochloride
CAS 23277-43-2

Related categories & resources

Browse the full Human APIs catalogue or all 560+ products. Reference documents: certifications portfolio · quality system · FDA DMF buyer guide · EU CEP supplier guide · complete product index.