API division produces under cGMP conditions Active ingredients and Drug intermediates both for own marketing and custom manufacturing. The unit is located about 220 km from Hyderabad enroute to Vijayawada at Jaggaiahpet, Krishna District.

The facility is inspected and approved by

  • Drug Control Administration of Andhra Pradesh
  • KFDA
  • PMDA Japan (Accredited)
  • EDQM
  • WHO GMP Certification

DMF’s have been filed with following authorities

  • Health Canada

Other Certifications:

  • Attained ISO 9001:2000 certificate from DET NORSKE VERITAS and upgraded to ISO 9001:2008


101 reactors, 8 clean rooms, robust team strength close to 346 dedicatedly working in operations catering more than 40 countries across the globe. The facility has 336 KL capacity, which is spread across

  • Hydrogenation Block
  • Corrosive Chemistry Block
  • Chemical Blocks
  • Technical Blocks and
  • Pharma Blocks with 100 K Facilities.

Pharma Blocks with 100 K Facilities.

facility is equipped with all kinds of process equipment with various capacities.

  • All Glass Reactors
  • Glass Line Reactors
  • SS Reactors
  • Hydrogenators
  • Centrifuges
  • Tray Driers
  • Vacuum Tray Driers
  • Fluid Bed Driers
  • Rotocone Vacuum Driers
  • Multi-mills
  • Sifters
  • Micronizers etc.

We have a dedicated Quality control laboratory within the premises with the following instruments.

  • HPLC
  • GC (Head Space)
  • FTIR
  • Polarimeter
  • UV-Visible Spectrophotometer
  • Stability Chambers
  • Muffle Furnace
  • KF Titrator