Theollex
Ammonium chloride, diphenylpyraline, etofylline, sodium citrate, theophylline
Every registration of this product has been cancelled.
Combination product
This product contains more than one active ingredient, so it has no single molecular structure.
Registration
- Applicants
- 1
- Registrations
- 1
Applicants and registrations
| Applicant | Brands | Dosages | Registrations | Schedule | Leaflets |
|---|---|---|---|---|---|
| Adcock ingram limitedCancelled | Theollex | Not stated | U0147 | Not determined | None |
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Theollex* EACH 30 ml CONTAINS AMMONIUM CHLORIDE 720 mg ANHYDROUS THEOPHYLLINE 100 mg DIPHENYLPYRALINE HYDROCHLORIDE 8 mg ETOFYLLINE 10 mg SODIUM CITRATE 300 mg | Not listed | U0147U/10.1/147 | 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.
Background
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.