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Lorlatinib (Lorbrena, Lorlatinib Pfizer)

Lorlatinib

Pfizer Laboratories (Pty) Ltd

Registration

Applicant
Pfizer Laboratories (Pty) Ltd
Registrations
4

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Lorbrena 25 MG

EACH TABLET CONTAINS LORLATINIB 25,0 mg

25 mg57009257/20.3/0092RegisteredNot determinedNone
Lorbrena 100 MG

EACH TABLET CONTAINS LORLATINIB 100,0 mg

100 mg57009357/20.3/0093RegisteredNot determinedNone
Lorlatinib 25 MG pfizer

EACH TABLET CONTAINS LORLATINIB 25,0 mg

25 mg570094.09257/20.3/0094.092RegisteredNot determinedNone
Lorlatinib 100 MG pfizer

EACH TABLET CONTAINS LORLATINIB 100,0 mg

100 mg570095.09357/20.3/0095.093RegisteredNot 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.

C21H19FN6O2406.40 g/mol

(16R)-19-Amino-13-fluoro-4,8,16-trimethyl-9-oxo-17-oxa-4,5,8,20-tetrazatetracyclo[16.3.1.02,6.010,15]docosa-1(22),2,5,10(15),11,13,18,20-octaene-3-carbonitrile

Drag to rotate. Structure from PubChem CID 71731823.

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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