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Morphine (Depodur)

Morphine

Pharmaplan (Pty) Ltd

Every registration of this product has been cancelled.

Registration

Applicant
Pharmaplan (Pty) Ltd
Registrations
3

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Depodur 10

EACH 1,0 ml SOLUTION CONTAINS MORPHINE SULPHATE 10,0 mg

1044011344/2.9/0113CancelledNot determinedNone
Depodur 15

EACH 1,5 ml SOLUTION CONTAINS MORPHINE SULPHATE 15,0 mg

1544108744/2.9/1087CancelledNot determinedNone
Depodur 20

EACH 2,0 ml SOLUTION CONTAINS MORPHINE SULPHATE 20,0 mg

2044108844/2.9/1088CancelledNot 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

  • S6: Morphine

    • except preparations and mixtures of morphine containing 0,2 percent or less of morphine, calculated as anhydrous morphine. (S2)

    Consolidated Schedules 06 July 2026, lines 10318 to 10319

  • S2: Morphine

    • mixtures containing 0,2 percent or less of morphine, calculated as anhydrous morphine.

    Consolidated Schedules 06 July 2026, line 2355

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.

C17H19NO3285.34 g/mol

(4R,4AR,7S,7aR,12bS)-3-methyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7,9-diol

Drag to rotate. Structure from PubChem CID 5288826.

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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