Codeine, guaifenesin, pseudoephedrine, triprolidine (Acutussive Adult Expect, Acutussive Paed Expect)
Codeine, guaifenesin, pseudoephedrine, triprolidine
Teva Pharmaceuticals (Pty) Ltd
Every registration of this product has been cancelled.
Registration
- Applicant
- Teva Pharmaceuticals (Pty) Ltd
- Registrations
- 2
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Acutussive adult expect EACH 5 ml SOLUTION CONTAINS CODEINE PHOSPHATE 7,5 mg GUAIFENESIN 100 mg PSEUDOEPHEDRINE HYDROCHLORIDE 20 mg TRIPROLIDINE HYDROCHLORIDE 1,25 mg | Not listed | X0010X/10.1/10 | Cancelled | Not determined | None |
| Acutussive paed expect EACH 5 ml SOLUTION CONTAINS CODEINE PHOSPHATE 3 mg GUAIFENESIN 50 mg PSEUDOEPHEDRINE HYDROCHLORIDE 12 mg TRIPROLIDINE HYDROCHLORIDE 0,6 mg | Not listed | X0011X/10.1/11 | 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.
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.
Combination product
This product contains more than one active ingredient, so it has no single molecular structure.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.