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Established 2007  ·  WHO-GMP certified

Medicine that reaches the last mile.

Affordable, quality-assured formulations manufactured to WHO-GMP standards and supplied to 4,200 pharmacies, hospitals and government health programmes.

6
Therapy areas in focus
240+
Formulations in the portfolio
18
Countries supplied
2
Manufacturing facilities
640
People across plants & field

Who we are

A generics manufacturer that treats quality as the product.

Medicare Pharma makes finished-dose generics for chronic and acute care. We began in 2007 with a single oral-solids line and now operate two facilities, an analytical development laboratory, and a distribution network reaching 18 countries.

Our work is unglamorous by design. A tablet has to dissolve the same way in month one and month thirty-six, in Bengaluru and in Kampala. That means validated processes, retained samples for every batch, stability chambers held at 25 °C/60% RH and 40 °C/75% RH, and documentation that survives an audit without anyone scrambling.

Therapeutic areas

Where our portfolio is concentrated

Six areas account for roughly 85% of dispatched volume. Each is supported by its own formulation team and dedicated stability programme.

Cardio-metabolic

Antihypertensives, statins, oral antidiabetics and fixed-dose combinations intended for long-term daily therapy.

  • Telmisartan
  • Metformin FDC
  • Rosuvastatin
  • Dapagliflozin

Anti-infectives

Broad-spectrum antibiotics, antifungals and antimalarials, including dispersible paediatric presentations.

  • Amoxicillin–Clav
  • Azithromycin
  • Cefixime DT
  • Fluconazole

Respiratory

Bronchodilators, leukotriene antagonists, antihistamines and mucolytic syrups for seasonal and chronic use.

  • Montelukast
  • Levocetirizine
  • Ambroxol syrup
  • Doxofylline

Gastro-intestinal

Proton pump inhibitors, prokinetics, enzyme preparations and ORS presentations for hospital and retail channels.

  • Pantoprazole
  • Rabeprazole–DSR
  • Ondansetron
  • ORS-L

Women’s health & nutrition

Haematinics, calcium and vitamin D combinations, prenatal supplements and therapeutic nutraceuticals.

  • Ferrous ascorbate
  • Calcium–D3
  • Methylcobalamin
  • Protein sachets

Dermatology & topicals

Creams, gels and ointments produced on a dedicated topicals line with segregated air handling.

  • Clobetasol
  • Ketoconazole
  • Mupirocin
  • Silver sulfadiazine

Research & development

Fourteen molecules moving through development

Development runs in defined stages. The bars show how far the current cohort of programmes has progressed through each one.

Stage 01

Product selection

  • Patent and exclusivity check
  • API sourcing and DMF review
  • Market and price modelling
Stage 02

Formulation development

  • Prototype trials at 1/10 scale
  • Comparative dissolution profiling
  • Excipient compatibility studies
Stage 03

Analytical & stability

  • Method development and validation
  • Accelerated 40 °C / 75% RH
  • Long-term 25 °C / 60% RH
Stage 04

Bioequivalence

  • Pilot study in fasted subjects
  • Pivotal study at a partner CRO
  • Statistical review of Cmax and AUC
Stage 05

Filing & scale-up

  • CTD dossier compilation
  • Exhibit batches at full scale
  • Regulatory queries and approval

Global presence

Eighteen countries, four export regions

Exports move through registered local partners who hold the marketing authorisation in their own market. We handle dossier support, artwork in local languages and shipment documentation.

India — domestic

Retail, hospital and institutional supply through 4,200 pharmacies and 38 stockists.

Primary market

East & West Africa

Kenya, Uganda, Tanzania, Nigeria, Ghana — anti-infectives and haematinics led.

5 countries

South-East Asia

Myanmar, Cambodia, Vietnam, Philippines — oral solids and topicals.

4 countries

Middle East

UAE, Oman, Yemen, Iraq — registration under review in two further markets.

4 countries

CIS & neighbours

Uzbekistan, Kyrgyzstan, Nepal, Sri Lanka — supplied against annual tenders.

4 countries

Looking for a manufacturing or supply partner?

Tell us the product, the volume and the market. We will come back with a feasibility note, an indicative cost and a realistic timeline.