Dabigatran Etexilate Mesylate pharmaceutical API powder — CAS 872728-81-9 — WHO-GMP manufacturer Longshine Boi-Tech, Pune, India
Human APIs

Dabigatran Etexilate Mesylate

CAS Registry Number: 872728-81-9

Dabigatran Etexilate Mesylate — active pharmaceutical ingredient (API) manufactured to pharmacopoeial specification. Purity ≥99.0%. CAS Registry Number: 872728-81-9. Supplied in bulk quantities from $1800.00/g entry for laboratory research,

Product information

Dabigatran Etexilate Mesylate — active pharmaceutical ingredient (API) manufactured to pharmacopoeial specification. Purity ≥99.0%. CAS Registry Number: 872728-81-9. Supplied in bulk quantities from $1800.00/g entry for laboratory research, analytical method development, and reference-standard applications.

Product specifications

CAS Registry Number
872728-81-9
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 Dabigatran Etexilate Mesylate-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.
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Frequently asked questions about Dabigatran Etexilate Mesylate

What is Dabigatran Etexilate Mesylate used for?

Dabigatran Etexilate Mesylate 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 Dabigatran Etexilate Mesylate typically reference it under CAS Registry Number 872728-81-9.

What quality and regulatory standards does Longshine Boi-Tech's Dabigatran Etexilate Mesylate meet?

Our Dabigatran Etexilate Mesylate 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 Dabigatran Etexilate Mesylate?

Quote requests for Dabigatran Etexilate Mesylate 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 Dabigatran Etexilate Mesylate to?

We export Dabigatran Etexilate Mesylate 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.

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Related categories & resources

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