Dextrose, anhydrous (Dextrose Fresenius, Fresenius ( ) Fresenius)
Dextrose, anhydrous
Fresenius Kabi Manufacturing SA (Pty) Ltd
Registration
- Applicant
- Fresenius Kabi Manufacturing SA (Pty) Ltd
- Certificate holder
- Fresenius Kabi Manufacturing SA (Pty) Ltd
- Registrations
- 5
- Schedule source
- SAHPRA documentation
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Dextrose 35% fresenius EACH 500 ml SOLUTION CONTAINS DEXTROSE, ANHYDROUS 175 g | 35%Solution for infusion. | 29055929/24/0559Approved 17 May 2022 | Registered | S3 | PIPIL |
| Dextrose fresenius 5% EACH 1 000,0 ml SOLUTION CONTAINS DEXTROSE, ANHYDROUS 50,0 g | 5%Solution for infusion. | C0228C/25.2/228Approved 17 May 2022 | Registered | S3 | PIPIL |
| Dextrose 50% fresenius EACH 500 ml CONTAINS DEXTROSE, ANHYDROUS 250 g | 50 mlSolution for infusion | L0196L/24/196Approved 13 May 2022 | Registered | S3 | PIPIL |
| Dextrose 20% fresenius EACH 500,0 ml SOLUTION CONTAINS DEXTROSE, ANHYDROUS 100,0 g | 20%Solution for infusion. | L0329L/24/329Approved 17 May 2022 | Registered | S3 | PIPIL |
| Fresenius 50 % (20 ml) injection fresenius EACH 20 ml AMPOULE CONTAINS DEXTROSE, ANHYDROUS 10 g | 50 % 20 mlInjection | V0222V/24/222 | Registered | Not determined | None |
Regulatory status
Where S3 sits on the scale
Needs a doctor's prescription, dispensed by a pharmacist.
Schedule 3 medicines can only be sold on a prescription from an authorised prescriber, such as a doctor or dentist. A pharmacist dispenses the medicine once they have the written prescription, or a verbal instruction from a prescriber they know. Its price, name, pack size and strength can still be told to the public, as long as nothing links it to what it treats.
Schedule S3, read from the product's PI-PIL leaflet.
Who may supply: A pharmacist dispensing against a written or verbal prescription from an authorised prescriber; a veterinarian, who may also prescribe, compound or dispense it directly; a medical practitioner or dentist, who may prescribe it and may compound or dispense it directly only if licensed under section 22C(1)(a); manufacturers and wholesalers may supply people who may lawfully possess it; and, for animal treatment, a person practising a para-veterinary profession, on a veterinarian's written or verbal instruction.
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
Schedule Verification
This medication's schedule (S3) has been verified from official SAHPRA documents with 90% confidence.
These documents are provided by SAHPRA for informational purposes. Always consult with a healthcare professional for medical advice.