The facility manufactures over 190 finished medicines across tablets, capsules, ointments, creams, and gels. It is internationally certified and supplies markets across Asia and Eastern Europe.
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Built for Sterile API Manufacturing
Validates SKUs
191
International Markets Served
04
Active Regulatory Approvals
05
Capabilities
Oral Solids Manufacturing
The site handles the full range of oral solid formats, from standard tablets and capsules through to sustained-release, modified-release, bilayered, and orally disintegrating tablets.
Tablets: uncoated, film-coated, enteric-coated, sustained-release, modified-release, bilayered, ODT
Capsules: enteric-coated pellets, sustained-release pellets, dual-pellet combinations
Dry-powder sachets for paediatric and effervescent formats
Semi-Solids Manufacturing
A dedicated suite handles all topical formats, operating independently from the oral solids floor with its own environmental controls.
Ointments, creams, gels, and lotions
Tube and bottle filling on-site
Packaging
Quality checks including leak testing, metal detection, and weight verification are built into every line.
Blister, strip, sachet, and tube formats
Three segregated finished-goods quarantine zones for release control
Quality Control
All testing is handled in-house, from raw materials through to finished product release.
Chemical analysis, dissolution testing, and microbiology
Long-term stability studies under internationally recognised conditions
Five external labs qualified for specialised testing
Approvals & Certifications
India / WHO scheme
(CDSCO / Tamil Nadu) India / WHO PQ
(Manufacturing Licence) India
(Cert. CDRR-CGMP-FA-179-01) Philippines
Belarus / EAEU
Sri Lanka
India / WHO scheme
(CDSCO / Tamil Nadu) India / WHO PQ
(Manufacturing Licence) India
(Cert. CDRR-CGMP-FA-179-01) Philippines
Belarus / EAEU
Sri Lanka
