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Uruguay · APIs

APIs supply to Uruguay

The APIs division counts 385 products, and each one can be quoted for delivery to Uruguay. Locally, the main users are in pulp & paper, meat & dairy processing and pharmaceuticals & veterinary products. Regular consignments go to industrial centres such as Montevideo, Fray Bentos and Paso de los Toros. Typical customers for this division are finished dosage formulators, generic dossier developers and veterinary drug manufacturers.

385products in this division
30–45 dsea transit from India
4–7 dair freight
10categories

Supplying APIs to Uruguay

By sea, containers and LCL lots take roughly 30–45 days to Montevideo and Nueva Palmira. Air cargo to Montevideo Carrasco (MVD) takes 4–7 days, which suits small and urgent packs. The relevant authority is MSP (Ministerio de Salud Pública). Our export desk lines up the COA, GHS SDS and shipping documents to match. Common grades for this division are IP, BP, USP and Ph. Eur..

Grades in this division

IPBPUSPPh. Eur.JP (on request)In-house / manufacturer specificationMicronised / particle-size specified

Pharma compliance in Uruguay

AuthorityMSP (Ministerio de Salud Pública)
SeaportsMontevideo, Nueva Palmira, Fray Bentos
AirportsMontevideo Carrasco (MVD)
Dangerous goodsIMDG by sea, IATA DGR by air

Medicines and APIs need registration or an import authorisation from the Ministry of Public Health (MSP), so confirm the importer's status before a pharmaceutical order ships. Precursor chemicals require a prior import licence, which the buyer obtains and shares with us so the commercial documents match. If goods enter a free zone or the Montevideo free port for later distribution, tell us at quotation stage so the consignee and paperwork are set up correctly. Dangerous goods are packed and declared under IMDG or IATA rules. Preferential MERCOSUR duty depends on a valid India–MERCOSUR PTA certificate of origin.

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. 30–45 daysOcean transit to Montevideo

    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 / MSP (precursor chemicals control).

Indicative total by sea: 37–62 days

By air: about 8–17 days in total.

Documents for Uruguay

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • Certificate of Origin in India–MERCOSUR PTA format for preferential duty
  • MSP import authorisation for pharmaceuticals where required
  • Precursor chemical import licence where applicable
  • Dangerous Goods Declaration (IMDG/IATA) where applicable

A selection we ship to Uruguay

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

Full APIs range
Questions

APIs for Uruguay

Do you ship APIs to Uruguay?
Yes. We ship by sea to Montevideo and Nueva Palmira, 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 APIs shipment to Uruguay?
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 MSP (Ministerio de Salud Pública) is agreed with you at quote stage.
How long does delivery to Uruguay take?
Allow 30–45 days for ocean transit or 4–7 days by air, plus packing, export clearance and import clearance. The timeline on this page shows each stage.
What information should I include when requesting an API quotation?
State the molecule, required pharmacopoeia and edition, quantity, intended use and destination country. Mention any special needs such as micronised particle size, a specific polymorph or limits on residual solvents. If your regulator needs manufacturer documents, list them too, so we can confirm availability before pricing.
Can you supply small API samples for formulation trials?
Many APIs can be supplied in development quantities for pre-formulation and stability work. The available sample size depends on the manufacturer and on how the molecule is regulated. Share your project stage and the amount you need, and we will advise what can ship as a sample and what requires a full commercial order.

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