PT Kalbe Farma Tbk
Southeast Asia's largest listed pharmaceutical and health supplement company.
PT Kalbe Farma Tbk is Indonesia's largest and Southeast Asia's largest publicly listed pharmaceutical and consumer health company, producing prescription drugs, OTC medicines, nutritional supplements, and functional health products under brands including Extra Joss, Fitbar, Diabetasol, and Prenagen. Kalbe International manages the group's export and cross-border trade across Southeast Asia and Africa, with facilities established in Nigeria to serve African markets. The company actively partners with wholesale distributors for its consumer health and nutritional supplement lines across ASEAN and beyond.
- Type
- Manufacturer
- Location
- Jakarta, Indonesia
- Founded
- 1966
- Website
- kalbe.co.id
- Categories
- Supplements & Wellness, Medical & Healthcare Supplies
- Markets
- Malaysia, Singapore, Vietnam, Thailand, Philippines, Nigeria, South Africa
Verified facts
- product-authorised-for-sale (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of products authorised for sale in Indonesia (Cek Produk)
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- domain-registered (green), checked 2026-08-08 Domain registry record
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- facility-registered (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of manufacturing facilities behind product registrations (Sarana)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)