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Medicines · US (FDA)
Antivirals

FDA 2017

Nucleoside and nucleotide reverse transcriptase inhibitors

Abacavir Sulfate and Lamivudine

Approved 28 Mar 2017OralTablet

The FDA lists this product in 10 strengths and forms.

Official labelAsk Osler about it

On this page

Composition
Strengths and forms
Official product information

The table holds no label text for this product yet, only the facts beside it. The official product information has the full text.

Composition

Active ingredients: ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletANDA090159-001 · Prescription
ABACAVIR SULFATE EQ 60MG BASE; LAMIVUDINE 30MG · Tablet, for suspensionNDA204311-001 · Discontinued
ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletANDA204990-001 · Prescription
ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletThis page
ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletANDA091144-001 · Prescription
ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletANDA205412-001 · Prescription
ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletANDA212663-001 · Discontinued
ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletANDA208990-001 · Discontinued

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Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletANDA216332-001 · Prescription

ABACAVIR SULFATE EQ 600MG BASE; LAMIVUDINE 300MG · TabletANDA079246-001 · Discontinued

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application ANDA206151.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Brand name: Abacavir Sulfate and Lamivudine
Active substance: abacavir sulfate
Drug class: Nucleoside and nucleotide reverse transcriptase inhibitors, Antivirals for treatment of HIV infections, combinations
Group: Antivirals
Route: Oral
Dosage form: Tablet
Applicant: Aurobindo Pharma
Status: Discontinued
FDA approval: 28 Mar 2017
Application: ANDA206151-001
RxCUI: 614534

Guidelines

Guidelines in infectious diseases1,342 guidelines in the library

FDA 2026

RilpivirineTablet

FDA 2025Emtricitabine and Tenofovir Alafenamideemtricitabine, tenofovir alafenamide · Tablet

FDA 2025Abacavir, Dolutegravir, LamivudineTablet

FDA 2025Bictegravir, Emtricitabine and Tenofovir AlafenamideTablet

FDA 2025Dolutegravir Sodium and Abacavir Sulfate and Lamivudineabacavir || dolutegravir || lamivudine · Tablet

FDA 2025Emtricitabine, Rilpivirine and Tenofovir Disoproxil Fumarateemtricitabine · Tablet

FDA 2024Emtricitabine and Tenofovir Alafenamide Fumarateemtricitabine · Tablet

FDA 2023PodofiloxGel

FDA 2023Dolutegravir; Emtricitabine; Tenofovir Alafenamidedolutegravir · Tablet

FDA 2023Dolutegravir; Rilpivirinedolutegravir · Tablet

FDA 2022PenciclovirCream

FDA 2022Trifluridine; Tipiraciltrifluridine · Tablet

FDA 2022Abacavir; Dolutegravir; Lamivudineabacavir · Tablet

FDA 2022Triumeq PDabacavir sulfate · Tablet, for suspension

FDA 2021Livtencitymaribavir · Tablet

FDA 2021Emtricitabine and Tenofovir Disoproxil Fumarateemtricitabine · Tablet