Emzor Pharmaceutical Industries Limited
Emzolyn, Emtrix ve geniş bir temel ilaç portföyünün Nijeryalı ilaç üreticisi.
Emzor Pharmaceutical Industries Limited, Nijerya sağlık pazarı için tabletler, şuruplar, merhemler ve enjekte edilebilir ürünler üretmektedir. Ürünleri öksürük şurupları, analjezikler, antimalaryaller ve besin takviyelerini içerir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Isolo, Nigeria
- Founded
- 1984
- Website
- https://www.emzorpharma.com
- Categories
- Takviyeler ve Sağlık, Tıbbi ve Sağlık Malzemeleri
- Markets
- Nijerya, Gana, Côte d’Ivoire
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- 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 2026-08-02 Internet Archive (Wayback)
Claimed certifications, not confirmed by us
- 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)