Sitagliptin (Metplitin)
Sitagliptin
Dr Reddyæs Laboratories (Pty) Ltd
Registration
- Applicant
- Dr Reddyæs Laboratories (Pty) Ltd
- Registrations
- 3
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Metplitin 25 MG EACH TABLET CONTAINS SITAGLIPTIN HYDROCHLORIDE MONOHYDRATE 25,0 mg | 25 mg | 56099656/21.2/0996 | Registered | Not determined | None |
| Metplitin 50 MG EACH TABLET CONTAINS SITAGLIPTIN HYDROCHLORIDE MONOHYDRATE 25,0 mg | 50 mg | 56099756/21.2/0997 | Registered | Not determined | None |
| Metplitin 100 MG EACH TABLET CONTAINS SITAGLIPTIN HYDROCHLORIDE MONOHYDRATE 100,0 mg | 100 mg | 56099856/21.2/0998 | 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.
(3R)-3-Amino-1-[3-(trifluoromethyl)-6,8-dihydro-5H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl]-4-(2,4,5-trifluorophenyl)butan-1-one
Drag to rotate. Structure from PubChem CID 4369359.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.