NDC 65862-026 – Lamivudine

Lamivudine 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-026

Product details

Brand name
Lamivudine
Generic name
Lamivudine
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077464
Marketed since
November 21, 2016
Listing expires
December 31, 2026
Pharmacologic class
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lamivudine →

Package NDC codes (2)

Package NDCDescriptionSince
65862-026-103 BLISTER PACK in 1 CARTON (65862-026-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKNov 21, 2016
65862-026-3030 TABLET, FILM COATED in 1 BOTTLE (65862-026-30)Nov 21, 2016

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