Our Facilities
State-of-the-art Facilities Designed to Meet Global Demand & Maximise Value
Our dedicated API and PFI manufacturing sites, Bonthapally and Jeedimetla continue to be strengthened through an increase in capacities and Regulatory accreditations. Through the acquisition of Auctus Pharmaceuticals (now Unit IV) in 2013, we took over a multi-product API manufacturing facility at Vizag and an intermediary manufacturing facility at Bonthapally both of which will augment our vision towards integration.
At Unit V, our Multi API facility, we manufacture small to medium volume APIs that are forward integrated into our finished dosages and sold to third party consumers.
Our Gagillapur unit is one of the largest single unit manufacturing site for PFIs and Finished Dosages which we are further adding to by increasing technology based capacities. In an effort towards forward integration, we set up a formulation R&D and manufacturing facility in Virginia, USA to develop and commercialize oral solid dosages in the US. This facility also gives us the ammunition to address any changes in the policies directed towards “Make in America.”
Bonthapally, Hyderabad
API Facility
- API Capacity: 34, 560 TPA
- 5 Paracetamol Grades
- 5.2 Ton Batch Size
- API - U.S. FDA, EDQM, WHO, COFEPRIS, INFARMED
- API Capacity: 175 KL PA
- Intermediate Facility
Jeedimetla, Hyderabad
Multi-Product API and PFI Facility
- API- 4,800 TPA
- PFI Capacity: 1,440 TPA
- 1.2 Ton PFI Batch Size
- API - U.S. FDA, EDQM, COFEPRIS, WHO, CDCSO
- PFI - WHO GMP, COFEPRIS, INFARMED
Gagillapur, Hyderabad
Finished Dosage and PFI Facility
- PFI Capacity: 24,000 TPA
- FD- 21.6 Bn PA
- 6 MT PFI Batch Size
- High Shear & Fluid Bed Granulation
- Pilot Facility with Geometrical Scale-Up
- PFI - US FDA, COFEPRIS, TGA, MCC, INFARMED
- FD - US FDA, MCC, COFEPRIS, TGA, INFARMED
Paravada (U-4), Visakhapatnam
API Facility
- API- 380 KL PA
- API - U.S. FDA, KFDA, EU GMP, WHO GMP, EDQM
Paravada (U-5), Visakhapatnam
API and FD Facility
- API Oncology- 4.33 KL & Non-Oncology / NPD- 10.53 KL.
- FD: Tablets-1Bn PA and Capsules- 71 Mn PA
- API & FDF - EU GMP
Chantilly, Virginia
R&D and FD Facility
- Capacity - 1.5 million units
- 100,000 Sq Feet – R&D & manufacturing capacity
- 1.5 Bn PA
- FD - US FDA, DEA
Genome Valley, Hyderabad
Granules Life Sciences
- 8 BN DOSAGE FD CAPACITY BY 2026