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Cilastatin (Imipenem/cilastatin Fresenius)

Cilastatin

Fresenius Kabi South Africa (Pty) Ltd

Every registration of this product has been cancelled.

Registration

Applicant
Fresenius Kabi South Africa (Pty) Ltd
Registrations
1

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Imipenem/cilastatin 250 mg/250 MG fresenius

EACH VIAL CONTAINS: IMIPENEM MONOHYDRATE EQUIVALENT TO IMIPENEM 250,0 mg CILASTATIN SODIUM EQUIVALENT TO CILASTATIN 250,0 mg

250 mg/250 mg47114947/20.1.1/1149CancelledNot determinedNone

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.

Listings for this ingredient that could not be applied to this product

  • S4: Cilastatin

    Consolidated Schedules 06 July 2026, line 5807

  • S4: Imipenem

    Consolidated Schedules 06 July 2026, line 6738

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.

C16H26N2O5S358.50 g/mol

(Z)-7-[(2R)-2-Amino-2-carboxyethyl]sulfanyl-2-[[(1S)-2,2-dimethylcyclopropanecarbonyl]amino]hept-2-enoic acid

Drag to rotate. Structure from PubChem CID 6435415.

SAHPRA documents

SAHPRA has not published a professional information or patient information leaflet for this product.

Background

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Research articles

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