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Codeine

Also known as: methylmorphine

Schedule 2 to 6, conditions apply
Loading the molecular structure
C18H21NO3299.40 g/mol

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

Drag to rotate; arrow keys step through the atoms. Structure from PubChem CID 5284371.

Listing

Schedules
Schedule 2 to 6, conditions apply
Source
Consolidated Schedules 06 July 2026

Registered medicines

34 registered products listed

Counted through the register's ingredient index, which does not reach every record.

Registered products
NameBrandsDosagesApplicantsRegistrationsSchedule
CodeineAmstil, Astrapain, Vacudol, +128 moretablets, 1 g, 1ml, 1 mg, +42 more49 applicants250 registrationsS6

6 more registered products name Codeine in their active ingredient

Registered products
NameBrandsDosagesApplicantsRegistrationsSchedule
Colzor AdultColzor adultNot statedAdcock ingram limited270436
Adco-neofed Paediatric CancelledAdco-neofed paediatricNot statedAdcock ingram limited270485
Neofed AdultNeofed adultNot statedAdcock ingram limited270486
Colzor Paediatric CancelledColzor paediatricNot statedAdcock ingram limited270487
Dinexol Paediatric Cough CancelledDinexol paediatric coughsyrupPharmacare limited û woodmead270530
Trifen Expect PaediatricTrifen expect paediatric5 mg/5 mlRanbaxy (SA) (Pty) Ltd270536S2
Trifen Expect AdultTrifen expect adult5 mlRanbaxy (SA) (Pty) Ltd270537S2
Flusin Junior CoughFlusin junior cough1 g, 5 mgPharmacare limited û woodmead280433
Flutex AntitussiveFlutex antitussiveNot statedPharmacare limited û woodmead280434
Zurituss Adult CancelledZurituss adultNot statedAdcock ingram limited280537
Zurituss Paediatric CancelledZurituss paediatricNot statedAdcock ingram limited280538
Tripofed PaediatricTripofed paediatricNot statedViatris South Africa (Pty) Ltd280681
Show the other 12 registered products
Registered products
NameBrandsDosagesApplicantsRegistrationsSchedule
Tripofed AdultTripofed adultNot statedViatris South Africa (Pty) Ltd290447
Endcol Paediatric Expectorant CancelledEndcol paediatric expectorantNot statedPharmacare limited û woodmeadT0255
Endcol ExpectorantEndcol expectorantNot statedPharmacare limited û woodmeadU0011
Acutussive Adult Expect CancelledAcutussive adult expectNot statedTeva Pharmaceuticals (Pty) LtdX0010
Acutussive Paed Expect CancelledAcutussive paed expectNot statedTeva Pharmaceuticals (Pty) LtdX0011
Innospect AdultInnospect adultNot statedInnovata pharmaceuticalsY0139
Innospect PaedInnospect paedNot statedInnovata pharmaceuticalsY0140
Expyn CancelledExpynNot statedThe Premier Pharmaceutical Co LtdB0807
Cetacod CancelledCetacodcapsulesThe Premier Pharmaceutical Co LtdB1456
Docsed CancelledDocsedNot statedPharmacare limited û woodmeadG0616
Pyracod CancelledPyracodsyrupThe Premier Pharmaceutical Co LtdG0893
CodefCodefsyrupUnimed Healthcare (Pty) LtdG1236

Regulatory status

Where S2 to S6 sits on the scale

Depends on which listing applies

At the least restrictive, Schedule 2: a pharmacist can sell it directly, without a prescription. At the most restrictive, Schedule 6: prescription-only, no repeats without a new prescription. The listings below say which applies to which form, strength or pack size.

Schedule S2 to S6, as the Consolidated Schedules list it.

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.

Consolidated Schedules listings for Codeine

  • S6: Codeine (methylmorphine)

    • single component codeine preparations;
    • oral solid preparations, in combination with one or more therapeutically active substances, in preparations not registered in terms of the Act, or when intended for export; (S2, S3)
    • liquid oral preparations and mixtures, in combination with one or more therapeutically active substances, in preparations not registered in terms of the Act, or when intended for export. (S2, S3)

    Consolidated Schedules 06 July 2026, lines 10128 to 10136

  • S3: Codeine (methylmorphine)

    • oral solid preparations, in combination with one or more therapeutically active substances, containing more than 10 milligrams of codeine (calculated as base) per dosage unit, when contained in products registered in terms of the Act, and not intended for export;
    • liquid oral preparations and mixtures, in combination with one or more therapeutically active substances, containing more than 10 milligrams of codeine (calculated as base) per 5 millilitre dosage unit, when contained in products registered in terms of the Act, and not intended for export;
    • except oral solid preparations, in combination with one or more therapeutically active substances, containing not more than 10 milligrams of codeine (calculated as base) per dosage unit, with a maximum daily dose not exceeding 80 milligrams, and in packs containing sufficient dosage units for a maximum treatment period of 5 days and limited to one pack per customer, when contained in products registered in terms of the Act, and not intended for export; (S2)
    • except liquid oral preparations and mixtures, in combination with one or more therapeutically active substances, containing not more than 10 milligrams of codeine (calculated as base) per 5 millilitre dosage unit, with a maximum daily dose not exceeding 80 milligrams, and with a pack size not exceeding 100 millilitres and limited to one pack per customer, when contained in products registered in terms of the Act, and not intended for export; (S2)
    • except single component codeine preparations. (S6)

    Consolidated Schedules 06 July 2026, lines 3350 to 3372

  • S2: Codeine (methylmorphine)

    • oral solid preparations, in combination with one or more therapeutically active substances, containing not more than 10 milligrams of codeine (calculated as base) per dosage unit, with a maximum daily dose not exceeding 80 milligrams, and in packs containing sufficient dosage units for a maximum treatment period of 5 days, and limited to one pack per customer, when contained in products registered in terms of the Act, and not intended for export;
    • liquid oral preparations and mixtures, in combination with one or more therapeutically active substances, containing not more than 10 milligrams of codeine (calculated as base) per 5 millilitre dosage unit, with a maximum daily dose not exceeding 80 milligrams, and with a pack size not exceeding 100 millilitres, when contained in products registered in terms of the Act, and not intended for export;
    • except oral solid preparations, in combination with one or more therapeutically active substances, containing more than 10 milligrams of codeine (calculated as base) per dosage unit; (S3)
    • except liquid oral preparations and mixtures, in combination with one or more therapeutically active substances, containing more than 10 milligrams of codeine (calculated as base) per 5 millilitre dosage unit; (S3)
    • except single component codeine preparations. (S6)

    Consolidated Schedules 06 July 2026, lines 1758 to 1778

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

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Research articles

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