Indofarma
Pharmazeutische Formulierungen, Generika und Gesundheitsprodukte.
Indofarma stellt in seinem Betrieb in Bekasi pharmazeutische Formulierungen, Generika und Gesundheitsprodukte her. Das Unternehmen beliefert Apothekenkanäle, Krankenhauseinkäufer, Vertriebshändler im Gesundheitswesen oder Exportkunden in seinen aufgeführten Hauptmärkten.
- Type
- brand seeking distribution
- Location
- Bekasi, Indonesia
- Founded
- 1918
- Website
- indofarma.id
- Categories
- Medizin- & Gesundheitsbedarf, Nahrungsergänzung & Wellness
- Markets
- Indonesien, Singapur, Malaysia, Philippinen
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
- domain-registered (green), checked 2026-08-08 Domain registry record
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- 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)