Ipratropium (Atrovent Hfa, Atrovent, Atrovent Udv, Atrovent D V)
Ipratropium
Ingelheim Pharmaceuticals (Pty) Ltd û Ferndale
Registration
- Applicant
- Ingelheim Pharmaceuticals (Pty) Ltd û Ferndale
- Registrations
- 4
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Atrovent 20 hfa EACH METERED DOSE CONTAINS IPRATROPIUM BROMIDE EQUIVALENT TO IPRATROPIUM BROMIDE ANHYDROUS 20,0 ug | 20 | 37027337/10.2.1/0273 | Registered | Not determined | None |
| Atrovent 0,025 % EACH 1 ml SOLUTION CONTAINS IPRATROPIUM BROMIDE 0,250 mg | 0,025 % | Q0117Q/10.2.1/117 | Cancelled | Not determined | None |
| Atrovent 0,5 udv EACH 2 ml VIAL CONTAINS IPRATROPIUM BROMIDE 0,5 mg | 0,5 | X0322X/10.2.1/322 | Cancelled | Not determined | None |
| Atrovent 0,25 u d v EACH 2 ml SOLUTION FOR INHALATION CONTAINS IPRATROPIUM BROMIDE 0,25 mg | 0,25 U | Z0038Z/10.2.1/38 | Cancelled | 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.
Listings for this ingredient that could not be applied to this product
S3: Ipratropium
- when contained in respirator solutions.
Consolidated Schedules 06 July 2026, line 3804
S2: Ipratropium
- except when contained in respirator solutions.
Consolidated Schedules 06 July 2026, line 2177
2 of 13 approved products with this ingredient carry S4 on their leaflet.
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.
[(1R,5S)-8-Methyl-8-propan-2-yl-8-azoniabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate
Drag to rotate. Structure from PubChem CID 657309.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.