Olopatadine (Olopatadine Eye FDC, Olovis, Zylopat)
Olopatadine
FDC SA (Pty) Ltd
Registration
- Applicant
- FDC SA (Pty) Ltd
- Registrations
- 3
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Olopatadine eye drops FDC EACH 1,0 ml SOLUTION CONTAINS OLOPATADINE HYDROCHLORIDE EQUIVALENT TO OLOPATADINE 1,0 mg | Drops | 56104956/15.4/1049 | Registered | Not determined | None |
| Olovis EACH 1,0 mg SOLUTION CONTAINS OLOPATADINE HYDROCHLORIDE EQUIVALENT TO OLOPATADINE 1,0 mg | Not listed | 561050.104956/15.4/1050.1049 | Registered | Not determined | None |
| Zylopat EACH 1,0 mg SOLUTION CONTAINS OLOPATADINE HYDROCHLORIDE EQUIVALENT TO OLOPATADINE 1,0 mg | Not listed | 561051.104956/15.4/1051.1049 | Registered | Not determined | None |
Regulatory status
This product is still scheduled by law even when this site could not determine which tier it falls under. The label carries the S number in a square border; ask a pharmacist if you need to know its schedule.
This is an informational summary of the Medicines and Related Substances Act 101 of 1965 and its 2017 General Regulations. It is not medical advice and not legal advice. Always check the medicine's label, which carries the schedule number inside a square border, or ask a pharmacist if you are unsure.
2-[(11Z)-11-[3-(Dimethylamino)propylidene]-6H-benzo[c][1]benzoxepin-2-yl]acetic acid
Drag to rotate. Structure from PubChem CID 5281071.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.