Preformulation Studies

Preformulation, or the physicochemical characterization of your Active Pharmaceutical Ingredient (API) in light of the intended route of administration and dosage form, is an important phase pharmaceutical development.

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Impurity Profiling

We have the combination of development expertise, manufacturing equipment and state-of-the-art facilities to be your strategic partner for reliable, cost effective long term supplies of your intermediates and API.

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Verification & Validation Services

Apnar's Validation Solutions group strives daily to provide superior service and support in a consistent, cost-effective manner 

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Analytical Method Development

As an integral part of product development, Apnar Pharma provides an analytical method development service. Additionally, Apnar Pharma also provides a standalone method development service, a method validation service, routine testing, and stability testing services in compliance with FDA/EMA and ICH guidelines. Apnar Pharma has experience in providing analytical services for regulatory submissions. We provide timely support for regulatory submissions and responding to regulatory deficiencies.

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Production Capability

New jersey, USA

  • Tablets - 1 Billion tablets/annum
  • Capsules(hard/soft) - 200 Million capsules/annum
  • Bottle Packaging - 2 Million bottles/annum
  • Blister Packaging - 85 Million Blister cards/annum
  • Secondary Packaging - Cartoning, Shrink Wrap, Bundling


  • Tablets- 275 Million tablets/annum
  • Capsules- 225 Million capsules/annum
  • Bottle Packaging - 16 Million bottles/annum