·PIB·15 marks·250–350 words

India remains heavily dependent on imported APIs despite being the 'pharmacy of the world.' Critically analyse government measures, including PRIP, to address this paradox.

In this answer
  1. Roots of the paradox
  2. Measures taken and what they have achieved
  3. Critical assessment

India supplies a large share of the world's generic medicines by volume, yet around two-thirds of its bulk drug and intermediate imports come from China [1] — a cost-driven dependence that makes the "pharmacy of the world" vulnerable at its own raw-material base. Government measures have narrowed this gap in parts, but have not yet dissolved the paradox.

Roots of the paradox

  • India's strength lies in formulation manufacturing, not upstream chemistry; scale economies, cheaper power and fermentation capacity moved KSM/API production to China [1].
  • Low R&D intensity kept firms in low-margin generics rather than original molecules, deepening reliance on imported inputs [5].

Measures taken and what they have achieved

  • PLI for KSMs/DIs/APIs: of 48 approved projects, 38 covering 28 products were commissioned by December 2025, creating about 56,800 MT of annual capacity and avoiding imports worth roughly ₹2,192 crore [1].
  • Bulk Drug Parks Scheme: three parks approved in Andhra Pradesh, Gujarat and Himachal Pradesh to supply shared utilities and cut conversion costs [2][3].
  • PRIP (2023-24 to 2027-28): a ₹5,000 crore Department of Pharmaceuticals scheme to shift the sector from cost-based to innovation-based growth, supporting about 300 projects worth ₹11,000 crore of R&D in new medicines, complex generics, biosimilars and devices, alongside Centres of Excellence at NIPERs [4][5]. Its second call opened in October 2025 after amendments to guidelines [4].

Critical assessment

  • Incentives are product-specific and time-bound; once subsidies taper, the Chinese cost advantage in fermentation-based APIs may reassert itself.
  • PRIP targets the innovation deficit, not import substitution directly — benefits are long-gestation, and the amendments signalled early implementation friction [4].
  • Bulk drug parks remain under construction, so capacity gains are still prospective [3].

Taken together, these schemes have shifted policy from incentivising volume to building capability — the correct direction. Sustaining it requires stable power and effluent infrastructure, predictable pricing, and stronger industry-NIPER research linkages, so that self-reliance in APIs becomes commercially self-sustaining rather than subsidy-dependent — the true test of Atmanirbhar Bharat in health security.

Sources

  1. 1APIs Imports from China, PIB (Department of Pharmaceuticals)two-thirds of bulk drug imports from China; PLI KSM/API project commissioning, 56,800 MT capacity, imports avoided
  2. 2Government measures to encourage domestic manufacturing in Pharmaceuticals, Bulk Drugs and Medical Devices, PIBBulk Drug Parks and PLI ecosystem-creation measures
  3. 3Centre grants 'in-principle' approval of three Bulk Drug Parks to Himachal Pradesh, Gujarat and Andhra Pradesh, PIBlocation and status of the three parks
  4. 4Call for proposals under PRIP scheme for industry & startup projects worth about ₹11,000 crore, PIBsecond call, October 2025 application window, amended guidelines
  5. 5PRIP Scheme aims to transform Indian Pharma-MedTech Sector through innovation-based growth, PIB₹5,000 crore outlay, ~300 projects, ₹11,000 crore R&D, CoEs at NIPERs, focus areas

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