NDC 65862-025 – Lamivudine

Lamivudine 150 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-025

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
65862-025-106 BLISTER PACK in 1 CARTON (65862-025-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKNov 21, 2016
65862-025-6060 TABLET, FILM COATED in 1 BOTTLE (65862-025-60)Nov 21, 2016

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