Hamdard Laboratories (Waqf) Pakistan
Hamdard Laboratories (Waqf) Pakistan is one of South Asia's largest Unani herbal medicine and wel…
Hamdard Laboratories (Waqf) Pakistan is one of South Asia's largest Unani herbal medicine and wellness product manufacturers, producing Rooh Afza syrup, herbal tonics, jams, honey, and a wide range of traditional medicines under the Hamdard brand. With manufacturing in Lahore and Karachi, the company exports to over 40 countries including the UK, UAE, Saudi Arabia, and North America, supplying diaspora grocery distributors and health food importers.
- Type
- Manufacturer
- Location
- Lahore, Pakistan
- Founded
- 1948
- Website
- hamdard.pk
- Categories
- Beverages, Supplements & Wellness, Medical & Healthcare Supplies
- Markets
- United Arab Emirates, Saudi Arabia, United Kingdom, United States, Canada, Australia
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-06 Mail server of the company domain
- registry-id-verified (green), checked 2026-08-19 FBR Active Taxpayer List (Federal Board of Revenue, Pakistan)
- registered-manufacturer (green), checked 2026-08-19 Pakistan Standards and Quality Control Authority (PSQCA), register of valid Certification Mark licences (local manufacturer scheme)
- sanctions-clear (green), checked 2026-08-06 OpenSanctions
- debarment-clear (green), checked 2026-08-06 OpenSanctions
Claimed certifications
- Halal Certified
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)