Skip to content

Finished formulations

Finished formulations from WHO GMP and EU GMP approved plants.

Finished dosage forms, from formulation development to supply: injectables, tablets, capsules, liquids, and dry powders, across OSD, general, cephalosporin, and beta-lactam lines. Sourced through our network of approved manufacturing partners in India, Latin America, and South Africa. We do not manufacture; we source, match, and manage.

What we source

Finished Formulations categories

Finished dosage forms, from formulation development to supply.

  • Injectables
  • Tablets and capsules (OSD)
  • Liquids
  • Dry powders
  • Topicals
  • Cephalosporins
  • Beta-lactams
  • General formulations

Across all major formulation types.

282 finished formulations are listed in the catalogue so far, each with its dosage form and strengths, and more are being added.

Browse the 282 formulations

What to send us for a quote

  • The product, its strength and dosage form
  • Pack size and pack style
  • Quantity, in units or packs
  • The destination market and what registration needs, such as a CTD or ACTD dossier or a CoPP
  • Your timeline

Have a specification sheet? Email it straight to our sales desk and we will take it from there.

End to end

How we support every engagement.

  • Supplier audit support

    Help evaluating and qualifying manufacturers.

  • Business development

    Matching demand to the right supply, and supply to demand.

  • QA / QC and dossier coordination

    Coordinating quality documentation and dossiers between the parties.

  • Documentation and paperwork

    Support with the trade paperwork a deal requires.

  • Payment terms

    Helping structure workable commercial terms between buyer and supplier.

  • Collection and logistics follow-up

    Staying with the shipment, chasing, and troubleshooting until it lands.

We coordinate and support; we do not assume the manufacturer's regulatory or quality responsibilities, and contracts of sale are directly between buyer and supplier.

How an order runs, stage by stage

Where we source

India

The core manufacturing base.

Latin America

EU-approved facilities.

South Africa

WHO GMP and PIC/S approved facilities.

We source exclusively from WHO GMP and EU GMP approved plants. Our partner facilities hold WHO GMP, EU GMP, ISO, and UK MHRA approvals. MH PharmaPack coordinates quality documentation between buyer and supplier; the approvals belong to the manufacturing partners.

Looking for a specific formulation?

Tell us the product, the dosage form and the market.