Nitrolith
Every registration of this product has been cancelled.
No structure available
This product's active ingredient could not be matched to a single known compound.
Registration
- Applicants
- 1
- Registrations
- 2
Applicants and registrations
| Applicant | Brands | Dosages | Registrations | Schedule | Leaflets |
|---|---|---|---|---|---|
| Adcock ingram limitedCancelled | Nitrolith | 250 mg, 500 mg | L0204, M0509 | Not determined | None |
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Nitrolith 500 MG EACH TABLET CONTAINS LITHIUM CARBONATE 500 mg | 500 mg | L0204L/2.6.5/204 | Cancelled | Not determined | None |
| Nitrolith 250 MG EACH TABLET CONTAINS LITHIUM CARBONATE 250 mg | 250 mg | M0509M/2.6.5/509 | 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.