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Sold as Abacavir And Lamivudine, Abacavir; Lamivudine. Every FDA application for this active ingredient: 3 branded and 1 generic.
As of Nov 15, 2026, FDA lists 4 applications for Abacavir;Lamivudine (sold as Abacavir And Lamivudine, Abacavir; Lamivudine), with 0 new uses approved and 0 published complete response letters.
First approved: not available
Applications: 4
New uses approved: 0
Complete response letters: 0
First approved in the EU: Dec 16, 2004
What Pharmacies Pay
Median price per unit across package codes in CMS's weekly NADAC survey, Nov 11, 2026, before rebates; see every drug's price change
ABACAVIR-LAMIVUDINE 600-300 MG: $1.43 per unitGeneric · -6% in a year
Approvals in the EU (EMA)
Centrally authorised medicines, matched by ingredient; see all EU approvals
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient.Drugs@FDA
Mylan Pharms Inc