Lark Laboratories
Indian pharmaceutical formulations manufacturer established in 1979 with in-house R&D and manufacturing for oral solids, liquids and topicals. Operates WHO-GMP-aligned quality systems, DSIR‑approved R&D centers, and exports products to multiple international markets. Offers formulation development of generics and complex/novel dosage forms and provides contract manufacturing and distribution to institutional customers.
Industries
Nr. of Employees
medium (51-250)
Lark Laboratories
A-105/2, Okhla Industrial Area, Phase-II, New Delhi-110020; Mon - Sat 9:00am - 6:00 pm
Products
Pharmaceutical formulation portfolio (by therapeutic area)
Range of finished pharmaceutical products across antibiotics, gynecology, gastroenterology, anti‑allergic, anti‑fungal, pediatrics, orthopedics, cardiovascular, anti‑diabetic, anti‑retroviral, anti‑psychotics and topical preparations.
Pharmaceutical formulation portfolio (by therapeutic area)
Range of finished pharmaceutical products across antibiotics, gynecology, gastroenterology, anti‑allergic, anti‑fungal, pediatrics, orthopedics, cardiovascular, anti‑diabetic, anti‑retroviral, anti‑psychotics and topical preparations.
Services
Development of generics and complex/novel formulations including process development and formulation optimization.
Development of generics and complex/novel formulations including process development and formulation optimization.
Expertise Areas
- Pharmaceutical formulation development
- Novel drug delivery systems (NDDS)
- Analytical development and microbiology testing
- WHO‑GMP quality systems and regulatory compliance
Key Technologies
- Formulation process chemistry
- Spray‑drying
- Taste‑masking techniques
- Drug‑layering
News & Updates
Company established in 1979 with multi‑decade history in pharmaceutical formulations manufacturing.
State‑of‑the‑art manufacturing unit set up in 2002 with facilities for OSD, liquids and topicals and a separate R&D facility.
Quality management systems aligned to WHO‑GMP and ISO 9001:2008 certification for manufacturing and quality processes.
R&D centers audited and approved by the Department of Scientific and Industrial Research (DSIR).
Products and facilities accredited/registered with regulators or ministries in multiple countries and presence in over 35 countries.
Company established in 1979 with multi‑decade history in pharmaceutical formulations manufacturing.
State‑of‑the‑art manufacturing unit set up in 2002 with facilities for OSD, liquids and topicals and a separate R&D facility.
Quality management systems aligned to WHO‑GMP and ISO 9001:2008 certification for manufacturing and quality processes.
R&D centers audited and approved by the Department of Scientific and Industrial Research (DSIR).
Products and facilities accredited/registered with regulators or ministries in multiple countries and presence in over 35 countries.