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VAQORACHEMICALS
Uruguay · APIs & Bulk Drugs

APIs & Bulk Drugs Supplier in Uruguay

Active pharmaceutical ingredients and bulk drugs sourced from Indian manufacturers, with COA, pharmacopoeial specs and regulatory documents on request. Formulation and generic manufacturers in Uruguay source APIs from us with batch COAs and, where the producing site holds them, DMF or CEP support.

385products in this division
30–45 dsea transit from India
4–7 dair freight
COA + SDSwith every lot

APIs & Bulk Drugs for Uruguay

The APIs and bulk drugs division supplies active pharmaceutical ingredients across major therapeutic classes, including anti-infectives, cardiovascular, antidiabetic, analgesic, gastrointestinal and CNS molecules. India is one of the world's largest API producing countries, and we source from manufacturers in established clusters such as Hyderabad, Vizag, Gujarat and Maharashtra.

Materials are offered to IP, BP, USP or Ph. Eur. monographs, or to in-house specifications where no monograph exists. Every shipment carries the manufacturer's batch COA and a GHS SDS. Depending on the product and the producing site, supporting documents such as a DMF letter of access, CEP, GMP certificate, EU written confirmation, TSE/BSE and residual solvent statements may be available. Availability is confirmed per product before you order, never assumed. We also help buyers assemble sample quantities for pre-qualification testing before a commercial order is placed.

Formulation manufacturers, generic companies developing dossiers, compounding and veterinary producers, and research groups needing reference quantities are the main buyers. Import of APIs is regulated in almost every market, so importers should confirm local licence, registration and site-approval requirements. We provide documents in the format the buyer's regulatory team requests where the manufacturer allows it.

Grades available

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

Compliance in Uruguay

Regulator: MSP (Ministerio de Salud Pública)

Medicines and APIs require registration or import authorisation from the Ministry of Public Health (MSP), and precursor chemicals are subject to prior import licensing. Uruguay's free zones and the free-port regime at Montevideo are widely used for regional distribution, and India–MERCOSUR PTA preferences need a valid certificate of origin. Dangerous goods must follow IMDG or IATA rules.

Shipping lanes

  • Montevideo
  • Nueva Palmira
  • Fray Bentos
  • Montevideo Carrasco (MVD)

Typical buyers: Finished dosage formulators, Generic dossier developers, Veterinary drug manufacturers, Nutraceutical and compounding companies, Pharma distributors and importers, R&D and pilot-scale labs.

Selected APIs & Bulk Drugs shipped to Uruguay

Full range
IP/BP/USP
Glimepiride chemical structure
Glimepiride
CAS
93479-97-1
Formula
C24H34N4O5S
MW
490.6 g/mol
VQ-004132
IP/BP/USP
Glipizide chemical structure
Glipizide
CAS
29094-61-9
Formula
C21H27N5O4S
MW
445.5 g/mol
VQ-004133
IP/BP/USP
Metformin HCl chemical structure
Metformin HCl
CAS
1115-70-4
Formula
C4H12ClN5
MW
165.62 g/mol
VQ-004135
IP/BP/USP
Mifepristone chemical structure
Mifepristone
CAS
84371-65-3
Formula
C29H35NO2
MW
429.6 g/mol
VQ-004137
IP/BP/USP
Norethisterone chemical structure
Norethisterone
CAS
68-22-4
Formula
C20H26O2
MW
298.4 g/mol
VQ-004139
IP/BP/USP
Orlistat chemical structure
Orlistat
CAS
96829-58-2
Formula
C29H53NO5
MW
495.7 g/mol
VQ-004140
IP/BP/USP
Prednisolone chemical structure
Prednisolone
CAS
50-24-8
Formula
C21H28O5
MW
360.4 g/mol
VQ-004141
IP/BP/USP
Progesterone chemical structure
Progesterone
CAS
57-83-0
Formula
C21H30O2
MW
314.5 g/mol
VQ-004142

FAQs — APIs & Bulk Drugs in Uruguay

Do you supply APIs & Bulk Drugs to Uruguay?

Yes. We export APIs & Bulk Drugs to Uruguay by sea freight to Montevideo or Nueva Palmira, by air cargo, or by express courier for small R&D packs. Every shipment includes a COA and a GHS SDS.

How long does delivery to Uruguay take?

Typical sea transit from India to Uruguay is 30–45 days and air freight 4–7 days, plus production/packing lead time and customs clearance.

Can you provide a DMF or CEP for an API?

It depends on the product and the manufacturing site. Where the manufacturer holds a US DMF, CEP or other filing, a letter of access or copy can often be arranged. We confirm availability per product before quoting.

Which pharmacopoeial standards do your APIs meet?

APIs are offered to IP, BP, USP or Ph. Eur. monographs as stated on the quotation and COA, and to manufacturer specifications where no monograph applies.

Do I need an import licence to buy APIs?

In most countries yes. Importers typically need a drug import or wholesale licence and sometimes site registration of the manufacturer. Please check requirements with your local regulator before ordering.

Other divisions for Uruguay

APIs & Bulk Drugs in nearby markets

APIs & Bulk Drugs quote — Uruguay

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