Azithromycin Dihydrate — active pharmaceutical ingredient (API) manufactured to pharmacopoeial specification. Purity ≥99.0% (HPLC). Physical form: White to off-white powder. CAS Registry Number: 117772-70-0. Supplied in 25g, 100g, 500g quantities from $95.00/g entry for laboratory research, analytical method development, and reference-standard applications.
We maintain regulatory dossiers in the following jurisdictions for Azithromycin Dihydrate-relevant molecules. Letter of Authorization (LoA) and CEP / DMF / ASMF references are issued at no charge to qualified buyers.
Yes — Longshine Boi-Tech holds regulatory documentation for Azithromycin Dihydrate (CAS 117772-70-0) covering FDA Type II DMF filing, EDQM CEP where applicable, and full stability data per ICH Q1A(R2). Ask our regulatory team for the current filing number and Letter of Access.
Azithromycin Dihydrate (CAS 117772-70-0) is quoted based on quantity, purity spec, and packaging. Contact sales@longshineboitech.com with your annual volume and target market — buyers filing DMFs typically get preferential pricing tied to committed offtake.
Azithromycin Dihydrate is manufactured to USP / Ph. Eur. / IP / JP grade as required by the buyer. Each lot ships with a Certificate of Analysis showing conformance to the selected monograph — HPLC identity, assay, related substances, residual solvents (ICH Q3C), and heavy metals (ICH Q3D).
We ship Azithromycin Dihydrate to buyers in 50+ countries across North America, Europe, Latin America, and Asia. Export requires the buyer to hold a valid pharmaceutical import authorisation in the destination country and, for controlled products, appropriate scheduling permits.
Standard MOQ for Azithromycin Dihydrate is scale-dependent — from 100 g for R&D pilots up to multi-kilogram commercial orders. Confirm current MOQ + lead time on the product quote request.
Azithromycin Dihydrate 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 Azithromycin Dihydrate typically reference it under CAS Registry Number 117772-70-0.
Our Azithromycin Dihydrate 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.
Quote requests for Azithromycin Dihydrate 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.
We export Azithromycin Dihydrate 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.
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.
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.