Sourcing loratadine tablets from China
Loratadine tablets from China fall within a tariff heading carrying 0% UK duty throughout. For routine commercial sale, settle the UK marketing authorisation before ordering and ask MHRA to confirm the applicable licence for import into Great Britain and any batch-certification requirements through the importer. Cambridge China Bridge sources loratadine tablets.

Zero duty on loratadine tablets
Heading 3004 covers medicines in measured doses or retail packs. For loratadine tablets, 3004 90 00 00 is the candidate line, subject to confirmation of the exact formulation. The table shows packaging variants under the same tariff line, rather than separate classifications. Give your broker the complete composition and packaging details when confirming the commodity code.
Read from the UK Trade Tariff on 10 October 2026, all supplied lines carry 0% duty for goods from China. The loratadine candidate line has no recorded anti-dumping or countervailing duty and no suspension. For another tablet family within this heading, see the cetirizine tablets guide.
The candidate line attaches controlled-drug, ozone-depleting-substance, CITES and seal-product import controls. Check applicability against the full formulation with your customs broker. Controlled drugs need licensing; listed species need CITES permits; regulated ozone-depleting substances need the applicable licence; seal products face a market ban with limited exceptions. The line also attaches controlled-drug, CITES, mercury and torture-and-repression export controls. Ask your broker to confirm requirements for any onward export.
| Goods | Commodity code | Duty | Anti-dumping or countervailing duty on China |
|---|---|---|---|
| Loratadine tablets in blister packs | 3004 90 00 00 | 0% | None |
Specify the authorised loratadine formulation
For routine commercial supply, loratadine tablets need a UK marketing authorisation. Ask MHRA to confirm the applicable licence for import from China into Great Britain and any batch-certification requirements involving the importer's Qualified Person. Before choosing the supplier, confirm the applicable good manufacturing practice requirements for the Chinese manufacturing site with MHRA and check its inspection history.
Specify loratadine as the active ingredient, the authorised strength, excipients, tablet appearance, any score line, pack configuration and approved storage conditions. Agree identity, assay, dissolution and impurity testing against the authorised specification. Review stability evidence, batch records and artwork together. Do not accept a different formulation or manufacturing site simply because the supplier calls it an equivalent tablet.
Worked duty example
Illustrative example, not a quote: Illustrative order of 500,000 loratadine tablets for a pharmaceutical wholesaler under 3004 90 00 00, invoiced at £80,000 free on board, with £4,000 of freight and insurance to the UK. The customs value is £84,000. Duty at 0% is £0. Import VAT at 20% is charged on the customs value plus duty, £84,000, so it is £16,800. With no duty, the only import tax is the VAT, which a VAT-registered importer can usually reclaim. The import duty and VAT guide explains each step.
Inspection checklist
Batch documents: match the certificate of analysis and executed batch records to the loratadine specification. Check identity, assay and dissolution results through the importer's quality system before batch certification.
Tablets and primary packs: check appearance against the agreed specification, look for chipped tablets and powder, and inspect blister seals or bottle closures for damage.
Cartons and leaflets: compare the medicine name, strength, warnings and leaflet with the approved artwork. Match legible batch numbers and expiry dates to the batch documents, and check carton Braille.
Shipment conditions: compare temperature records with the labelled storage conditions. Check seals, carton condition and quantities against dispatch documents before the importer reviews the consignment for release.
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What goes wrong
An acceptable sample does not establish that the production batch meets the authorised loratadine specification. Problems include drifting assay or dissolution results, incomplete batch records and a manufacturing site that does not match the authorisation. Treat a change of excipient, tablet shape or primary packaging as a matter for the buyer's pharmaceutical quality team before accepting it.
Packs can arrive with the wrong strength printed on the foil, mismatched batch numbers or an outdated leaflet. Transit damage and missing temperature records create further uncertainty. Keep affected stock separate while the licensed importer investigates, and settle document and artwork discrepancies before release.
Cambridge China Bridge sources these products for UK businesses, checking the factory and the documents before shipment. See factory verification. For repeat volumes, see container programmes.
Frequently asked questions
What is the UK import duty on loratadine tablets from China?
The candidate code 3004 90 00 00 carries 0% duty in the supplied tariff facts, with no recorded anti-dumping or countervailing duty and no suspension. Confirm the exact formulation and attached controls.
Do I need a licence to import loratadine tablets from China?
For import into Great Britain, ask MHRA to confirm which licence covers import from China and whether you should hold it yourself or work through a licensed importer. Confirm the applicable batch-certification arrangements with MHRA and the importer.
Can I sell Chinese loratadine tablets under my own brand?
For routine commercial sale, the product needs a UK marketing authorisation. Settle the formulation, manufacturing site and approved packaging before commissioning own-brand stock.
What should I check when loratadine tablets arrive?
Match batch documents, strength, pack artwork and expiry dates. Inspect tablets and seals, review temperature records, and have the licensed importer complete the batch-release checks.