Zota Health Care Ltd.
Produits pharmaceutiques génériques et nutraceutiques
Zota Health Care fabrique et commercialise des médicaments génériques sur ordonnance et des produits nutraceutiques en vente libre. Son usine certifiée GMP du Gujarat produit des comprimés, des capsules et des liquides oraux pour le marché indien. L'entreprise distribue ses produits via un réseau national de pharmacies.
- Type
- brand seeking distribution
- Location
- Surat, India
- Founded
- 1992
- Website
- https://www.zotahealthcare.com
- Categories
- Compléments et bien-être, Fournitures médicales et de santé
- Markets
- Inde
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- domain-registered (green), checked 2026-08-10 Domain registry record
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-activity (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
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)