FLUDARABINE PHOSPHATE POWDER FOR SOLUTION FOR INJECTION INFUSION USP Singapore - English - HSA (Health Sciences Authority)

fludarabine phosphate powder for solution for injection infusion usp

fresenius kabi (singapore) pte ltd - fludarabine phosphate usp - injection, powder, for solution - fludarabine phosphate usp 50 mg/ vial

TEVA-FLUDARABINE 25 TABLET South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

teva-fludarabine 25 tablet

teva pharmaceuticals (pty) ltd - tablet - see ingredients - each 2,0 ml vial contains fludarabine phosphate 50,0 mg

Fludara New Zealand - English - Medsafe (Medicines Safety Authority)

fludara

sanofi-aventis new zealand limited - fludarabine phosphate 25 mg/ml;   - powder for injection - 50 mg/2ml - active: fludarabine phosphate 25 mg/ml   excipient: mannitol sodium hydroxide

Fludara oral New Zealand - English - Medsafe (Medicines Safety Authority)

fludara oral

pharmacy retailing (nz) ltd t/a healthcare logistics - fludarabine phosphate 10mg - film coated tablet - 10 mg - active: fludarabine phosphate 10mg excipient: colloidal silicon dioxide croscarmellose sodium hypromellose iron oxide red iron oxide yellow lactose monohydrate magnesium stearate microcrystalline cellulose purified talc titanium dioxide - the treatment of b-cell chronic lympocytic leukaemia.

Fludara 10 mg film-coated tablets Ireland - English - HPRA (Health Products Regulatory Authority)

fludara 10 mg film-coated tablets

genzyme europe b.v. - fludarabine phosphate - film-coated tablet - 10 milligram(s) - purine analogues; fludarabine