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Lamivudine — Discount Pricing

Lamivudine is not confirmed for no-additional-cost pricing. Discount pricing may be available; confirm the price with the dispensing pharmacy.

Lamivudine Pricing

Pricing typePrice
TheDrugClubDiscount pricing may be available
Typical Retail$128.00

Discount pricing may be available; confirm the price with the dispensing pharmacy.

About Lamivudine

Lamivudine is a prescription medication. Ask your doctor if Lamivudine is right for you.

Combination products containing Lamivudine

How to Check Lamivudine Pricing

  1. Join TheDrugClub for $19.95/month
  2. Receive your member card by email
  3. Present your card at a participating pharmacy
  4. Check active-formulary eligibility or available discount pricing

Lamivudine at Participating Pharmacies

Pharmacy participation and fulfillment options vary. Present your membership card and confirm current pricing before filling.

Other medications in Infections

About Lamivudine

Lamivudine is a vital medication used to manage chronic viral infections like HIV and Hepatitis B. Understanding its role in your health journey is crucial, and so is finding affordable access. With TheDrugClub, members can often discover significant savings on essential prescriptions like lamivudine, helping to make your treatment more manageable.

Lamivudine, often known by its brand name Epivir or Epivir-HBV, is an antiviral medication prescribed to combat two significant viral infections: Human Immunodeficiency Virus (HIV) and chronic Hepatitis B virus (HBV) infection. For HIV, it's typically used as part of a combination therapy, helping to reduce the amount of virus in the body and improve the immune system. For chronic Hepatitis B, it works to slow down the progression of the disease and reduce liver damage.

Lamivudine belongs to a class of drugs called nucleoside reverse transcriptase inhibitors (NRTIs). When HIV or HBV replicates, they use an enzyme called reverse transcript

The information above is for educational purposes only and does not constitute medical advice. Consult your healthcare provider before making medication decisions.

What Lamivudine is approved for (FDA label)

Lamivudine tablets (HBV) are indicated for the treatment of chronic hepatitis B virus (HBV) infection associated with evidence of hepatitis B viral replication and active liver inflammation [see Clinical Studies ( 14.1 , 14.2 )]. The following points should be considered when initiating therapy with lamivudine tablets (HBV): • Due to high rates of resistance development in treated patients, initiation of treatment with lamivudine tablets (HBV) should only be considered when the use of an alternative antiviral agent with a higher genetic barrier to resistance is not available or appropriate. • Lamivudine tablets (HBV) have not been evaluated in patients co-infected with human immunodeficiency virus (HIV), hepatitis C virus (HCV), or hepatitis delta virus.

Source: Read the full FDA label on DailyMed. Label effective date: July 29, 2026.

Excerpt from the FDA-approved prescribing information. This is not medical advice; talk to your doctor or pharmacist.

Boxed warning for Lamivudine (FDA label)

WARNING: EXACERBATIONS OF HEPATITIS B and RISK OF HIV-1 RESISTANCE IF LAMIVUDINE TABLETS (HBV) IS USED IN PATIENTS WITH UNRECOGNIZED OR UNTREATED HIV-1 INFECTION Severe acute exacerbations of hepatitis B have been reported in patients who have discontinued anti-hepatitis B therapy (including lamivudine tablets (HBV). Hepatic function should be monitored closely with both clinical and laboratory follow-up for at least several months in patients who discontinue anti-hepatitis B therapy. If appropriate, initiation of anti-hepatitis B therapy may be warranted [see Warnings and Precautions (5.1) ]. Lamivudine tablets (HBV) are not approved for the treatment of human immunodeficiency virus type 1 (HIV-1) infection because the lamivudine dosage in lamivudine tablets (HBV) is subtherapeutic and monotherapy is inappropriate for the treatment of HIV-1 infection. HIV-1 resistance may emerge in chronic hepatitis B-infected patients with unrecognized or untreated HIV-1 infection. HIV counseling and testing should be offered to all patients before beginning treatment with lamivudine tablets (HBV) and periodically during treatment [see Warnings and Precautions (5.2) ]. WARNING: EXACERBATIONS OF HEPATITIS B and RISK OF HIV-1 RESISTANCE IF LAMIVUDINE TABLETS (HBV) IS USED IN PATIENTS WITH UNRECOGNIZED OR UNTREATED HIV-1 INFECTION See full prescribing information for complete boxed warning • Severe acute exacerbations of hepatitis B have been reported in patients who have discontinued anti-hepatitis B therapy (including lamivudine tablets (HBV).

Source: FDA prescribing information (DailyMed). Set ID: 6bd6b9da-df69-46db-813e-4e7f3bdecf95. SPL document ID: 57c05c90-abd7-b7ab-e063-6394a90a93db. Label effective date: July 29, 2026. Read the full label.

Excerpt from the FDA-approved prescribing information. This is not medical advice; talk to your doctor or pharmacist.

Dosage forms and strengths for Lamivudine (FDA label)

• Lamivudine tablets (HBV): 100 mg are pink colored, capsule shaped, biconvex, film coated tablets, debossed with ‘37’ on one side and ‘I’ on the other side. • Tablets: 100 mg ( 3 )

Source: FDA prescribing information (DailyMed). Set ID: 6bd6b9da-df69-46db-813e-4e7f3bdecf95. SPL document ID: 57c05c90-abd7-b7ab-e063-6394a90a93db. Label effective date: July 29, 2026. Read the full label.

Excerpt from the FDA-approved prescribing information. This is not medical advice; talk to your doctor or pharmacist.

Adverse reactions for Lamivudine (FDA label)

The following adverse reactions are discussed in other sections of the labeling: • Exacerbations of hepatitis B after discontinuation of treatment [see Warnings and Precautions (5.1) ]. • Risk of emergence of resistant HIV-1 infection [see Warnings and Precautions (5.2) ]. • Risk of emergence of resistant HBV infection [see Warnings and Precautions (5.3) ]. • Lactic acidosis and severe hepatomegaly with steatosis [see Warnings and Precautions (5.4) ]. The most common reported adverse reactions in those receiving lamivudine tablets (HBV) (incidence greater than or equal to 10% and reported at a rate greater than placebo) were ear, nose, and throat infections; sore throat; and diarrhea. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Hetero Labs Limited at 1-866-495-1995 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared with rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.

Source: FDA prescribing information (DailyMed). Set ID: 6bd6b9da-df69-46db-813e-4e7f3bdecf95. SPL document ID: 57c05c90-abd7-b7ab-e063-6394a90a93db. Label effective date: July 29, 2026. Read the full label.

Excerpt from the FDA-approved prescribing information. This is not medical advice; talk to your doctor or pharmacist.

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