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Fylibix

Active ingredient not listed in the SAHPRA register

Sandoz South Africa (Pty) Ltd

Every registration of this product has been cancelled.

Registration

Applicant
Sandoz South Africa (Pty) Ltd
Registrations
5

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Fylibix 20

Dasatinib

2055057455/26/0574CancelledNot determinedNone
Fylibix 50

Dasatinib

5055057555/26/0575CancelledNot determinedNone
Fylibix 70

Dasatinib

7055057655/26/0576CancelledNot determinedNone
Fylibix 80

Dasatinib

8055057755/26/0577CancelledNot determinedNone
Fylibix 100

Dasatinib

10055057855/26/0578CancelledNot 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.

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.

No structure available

The SAHPRA register lists no active ingredient for this product, so there is no compound to show.

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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