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Lebanon · Pharmaceutical Intermediates

Pharmaceutical Intermediates for Lebanon

Buyers in Lebanon can order any of the 14,468 products in our pharmaceutical intermediates division. In Lebanon the strongest demand is from pharmaceutical manufacturing, cosmetics & personal care and paints & coatings. Regular consignments go to industrial centres such as Beirut, Mount Lebanon industrial zones and Tripoli. Typical customers for this division are API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

14,468products in this division
18–26 dsea transit from India
3–6 dair freight
4categories

Supplying pharmaceutical intermediates to Lebanon

By sea, containers and LCL lots take roughly 18–26 days to Beirut and Tripoli. Air cargo to Beirut–Rafic Hariri (BEY) takes 3–6 days, which suits small and urgent packs. The relevant authority is Ministry of Public Health. Our export desk lines up the COA, GHS SDS and shipping documents to match. Common grades for this division are Key starting material (KSM) specification, Advanced intermediate (customer spec), Building block, ≥95% / ≥98% purity and Chiral (ee specified).

Grades in this division

Key starting material (KSM) specificationAdvanced intermediate (customer spec)Building block, ≥95% / ≥98% purityChiral (ee specified)Technical gradeLow genotoxic-impurity specification

Pharma compliance in Lebanon

AuthorityMinistry of Public Health
SeaportsBeirut, Tripoli
AirportsBeirut–Rafic Hariri (BEY)
Dangerous goodsIMDG by sea, IATA DGR by air

Hazardous and dual-use chemicals usually need prior import approval, with the Ministry of Environment and other ministries involved depending on the substance. APIs and medicines are regulated by the Ministry of Public Health, which typically requires product registration and batch documentation. Given the economic situation, settlement is commonly in US dollars and payment terms should be agreed in writing before goods leave India. Keep approvals, invoices and the COA consistent so clearance in Beirut is not delayed. Dangerous goods follow IMDG or IATA rules.

From order to delivery

  1. 1–2 daysQuote and document set agreed

    Price, pack sizes, Incoterm and the paperwork list are confirmed in writing.

  2. 3–7 daysPacking for export

    Stock items are packed in UN-rated drums or cartons. Made-to-order material adds its own lead time.

  3. 1–3 daysExport clearance at Nhava Sheva or Mundra

    Shipping bill filed, dangerous goods declared under IMDG where needed.

  4. 18–26 daysOcean transit to Beirut

    Port-to-port time depends on the vessel schedule and any transhipment.

  5. 2–5 daysImport clearance

    Your broker clears the goods against local rules. Chemical oversight: Ministry of Environment.

Indicative total by sea: 25–43 days

By air: about 7–16 days in total.

Documents for Lebanon

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • Prior import approval for hazardous/controlled chemicals
  • Ministry of Public Health approval for APIs where applicable
  • Dangerous Goods Declaration (IMDG/IATA) where applicable

A selection we ship to Lebanon

A rotating sample from the division. Every product in the catalogue can be quoted for this destination.

Full pharmaceutical intermediates range
Questions

Pharmaceutical Intermediates for Lebanon

Do you ship pharma intermediates to Lebanon?
Yes. We ship by sea to Beirut and Tripoli, by air cargo or by express courier depending on quantity and urgency. Every lot carries a COA and a 16-section GHS SDS.
Which documents come with a pharma intermediates shipment to Lebanon?
Commercial invoice, packing list, certificate of analysis and SDS as standard, plus the bill of lading or air waybill and a certificate of origin. Anything specific to Ministry of Public Health is agreed with you at quote stage.
How long does delivery to Lebanon take?
Allow 18–26 days for ocean transit or 3–6 days by air, plus packing, export clearance and import clearance. The timeline on this page shows each stage.
Can you scale an intermediate from grams to kilograms without changing the route?
For many listed intermediates the gram packs and the kilogram supply come from the same manufacturing route, which keeps the impurity profile consistent. Where scale-up needs a different route, we tell you before you commit and can provide comparison samples so your team can check the new material against the old.
How do you control isomer and enantiomer content?
Positional isomers are controlled by HPLC or GC methods suited to the compound, and chiral intermediates are tested by chiral HPLC to report enantiomeric excess. The limits that apply to your lot appear on the COA. If your process needs tighter limits, state them on the enquiry and we will confirm what can be met.

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