To Improving affordable healthcare
globally

Injectable manufacturer focuses on CDMO, our experience CDMO expertise enable us to collaborative strategies and commitment

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Experience

About us

Who We Are

Sai Parenterals Limited is a diversified pharmaceutical formulations company with expertise in research, development, and manufacturing. We operate across two business verticals

  • Branded Generic Formulation
  • Contract Development & Manufacturing Organisation (CDMO) services

Our portfolio spans multiple therapeutic areas including cardiovascular, neuropsychiatry, anti-diabetic, respiratory health, antibiotics, gastroenterology, vitamins, minerals & supplements (VMS), analgesics, and dermatology. We manufacture products across dosage forms such as injectables, tablets, capsules, liquid orals, and ointments, developed through in-house R&D and strategic acquisitions.

In the injectables segment, we have sterile manufacturing capabilities for critical care and penicillin-based therapies, with delivery systems including dry powder injections, pre-filled syringes, ampoules, and vials.

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Businesses & Products

What We Do

In the injectables segment, we have sterile manufacturing capabilities for critical care and penicillin-based therapies, with delivery systems including dry powder injections, pre-filled syringes, ampoules, and vials.

Research & Innovation

How We Work

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Branded Generic Formulations

We serve a diverse domestic customer base, including central and state government agencies, pharmaceutical companies, institutions, and super stockists.

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CDMO Products and Services

Our CDMO business vertical provides end-to-end solutions covering product development, regulatory dossier preparation, international filings, validation batches, and commercial manufacturing.

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Manufacturing Capabilities

We have four (4) Manufacturing Facilities based in Hyderabad, Telangana, including two dedicated to injectables, a solid oral dosage facility, and a dedicated cephalosporin facility.

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Get In Touch

his gives your visitors confidence that you have a structured, professional process and builds credibility.

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Product Development

Complex generics, value-added formulations, alternate dosage forms

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Regulatory Strength

Dossier preparation, international filings, compliance with global standards

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Global Reach

Supplying to regulated and semi-regulated markets across Australia, New Zealand, Southeast Asia, Middle East, and Africa

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